United States Court of Appeals,

                                         Eleventh Circuit.

                                           No. 97-5801.

                              Lisa GOODLIN, Plaintiff-Appellant,

                                                 v.

                           MEDTRONIC, INC., Defendant-Appellee.

                                          Feb. 18, 1999.

Appeal from the United States District Court for the Southern District of Florida. (No. 97-6133-CIV-
FAM), Federico A. Moreno, Judge.

Before TJOFLAT and EDMONDSON, Circuit Judges, and KRAVITCH, Senior Circuit Judge.

       KRAVITCH, Senior Circuit Judge:

       This appeal requires us to determine the preemptive effect of the Medical Device

Amendments ("MDA"), 21 U.S.C. § 360c et seq., to the Federal Food, Drug and Cosmetic Act

("FDCA"), 21 U.S.C. § 301 et seq. Lisa Goodlin brought suit against Medtronic, Inc. ("Medtronic"),

alleging that her Medtronic cardiac pacemaker lead was defective in a way that gave rise to two

causes of action under Florida common law. Medtronic argues that because the United States Food

and Drug Administration (the "FDA") approved the device pursuant to the MDA's premarket

approval process, section 360k(a) of the MDA preempts Goodlin's state law claims. The district

court agreed and granted summary judgment to Medtronic. We reverse.

                                        BACKGROUND

       In January 1991, Goodlin received a Medtronic pacemaker and its related components,

including Medtronic's 4004/M lead.         The pacemaker lead is a wire that transmits the

heartbeat-steadying electrical impulse from the pulse generator to the heart. Goodlin depends on

the pacemaker to support her life.
       The FDA approved Medtronic's 4004/M lead for use in the United States on February 10,

1989. Sometime after Goodlin received her pacemaker, however, an FDA inspection revealed a

significant risk that the 4004/M lead would fail due to degradation of the lead's polyurethane

insulating material. The FDA, therefore, instructed Medtronic to issue a Health Safety Alert letter

to inform physicians about the risk of defect in the lead. The letter advised physicians to consider

prophylactic replacement for pacemaker dependent patients and advised them to replace the lead if

the risk of its continued use outweighed the risks associated with its replacement. Upon the advice

of her physician, Goodlin underwent open-heart surgery to replace the lead. The lead that the

surgeons removed from Goodlin showed no signs of failure.

        Goodlin brought suit against Medtronic in 1997. Her amended complaint asserts claims for

negligent design and strict product liability, both of which arise under Florida common law.

Medtronic moved for summary judgment on the basis of federal preemption, arguing that section

360k(a) of the MDA expressly preempted Goodlin's claims. The district court found that because

the FDA had reviewed and approved the safety and effectiveness of the 4004/M device pursuant to

its premarket approval process, the MDA preempted Goodlin's claims. The court, therefore, entered

summary judgment in Medtronic's favor. We review the district court's decision to grant summary

judgment on the issue of preemption de novo and apply the same standards that bound the district

court. See Lewis v. Brunswick Corp., 

, 1498 (11th Cir.), cert. granted, --- U.S. ----,

, 

(1997), cert. dismissed, --- U.S. ----, 

, 

(1998).

                                          DISCUSSION

I. Regulatory Overview


                                                 2
        Despite the historical prominence of the states in matters concerning the health and safety

of their citizens, the federal government has expanded its role in this field over the past century. See

Medtronic, Inc. v. Lohr, 

, 475, 

, 2245-56, 

(1996)

(providing a survey of the federal government's legislation in this area). In the 1970s, against the

backdrop of several highly publicized events involving defective medical devices, including the

tragedies connected to the Dalkon Shield intrauterine device, Congress turned its attention to the

regulation of medical devices. 

116 S.Ct. at 2246. In 1976, Congress passed the MDA,

the statute at issue here, which categorizes medical devices according to the risk they pose to the

public. The MDA classifies devices that either "present a potential unreasonable risk of illness or

injury" or that are "purported or represented to be for a use in supporting or sustaining human life

or for a use which is of substantial importance in preventing impairment of human health" as Class

III devices. 

116 S.Ct. at 2246 (quoting 21 U.S.C. § 360c(a)(1)(C))(internal quotation

omitted). Pacemakers, such as the one at issue here, are Class III devices. See 21 C.F.R. §

870.3610(b).

A. The Premarket Approval Process

        Before a manufacturer can introduce a new Class III medical device into the marketplace,

the manufacturer must provide the FDA with a "reasonable assurance" that the device is both safe

and effective. 21 U.S.C. § 360c(a)(1)(C). Manufacturers may furnish this assurance through the

FDA's premarket approval process, commonly referred to as the "PMA" process.1 As the Supreme


   1
    The MDA permits manufacturers to avoid the PMA process by obtaining approval for
devices introduced to the market before May 28, 1976, when the MDA took effect. See 21
U.S.C. § 360e(b)(1)(A); 21 C.F.R. § 814.1(c)(1). A manufacturer may also seek approval of a
new device by showing that the new device is the "substantial equivalent" of such a
grandfathered device. See 21 U.S.C. § 360e(b)(1)(B)(ii). The FDA's review for substantial

                                                   3
Court observed in Lohr, and as Medtronic has reminded us in its briefs, the PMA process is rigorous

because it permits the FDA to demand the submission of detailed information regarding the safety

and effectiveness of the device under review.2 See 21 U.S.C. § 360e(c)(1) (describing the required

contents of a PMA application). The FDA then spends substantial time and resources reviewing

these applications; indeed, the average submission requires 1,200 hours of review. See Lohr, 518

U.S. at 

-47. Ordinarily, the FDA refers the device to an independent panel

of experts, which prepares a report and recommendation on whether to approve the device. See 21

U.S.C. § 360e(c)(2). The FDA may also advise an applicant of deficiencies in the PMA application

and notify the applicant of any measures necessary to put the application in approvable form. 

Once the FDA determines that the manufacturer has provided the required reasonable

assurances, the agency issues an order that permits the manufacturer to market the device, exactly

as approved. Thereafter, the manufacturer may not change the approved labeling, product design,

or manufacturing process in any way that would affect the safety or effectiveness of the device. See




equivalence, dubbed the "510k process" in reference to its section number in the original Act, is
limited in scope. Instead of the extensive inquiry into safety and effectiveness contemplated in
the PMA process, the FDA completes the average 510k review within 20 hours, and the agency
considers only whether the device is indeed the equivalent of a preexisting device—regardless of
how unsafe or ineffective the grandfathered device happens to be. See generally 

, 116 S.Ct. at 2247-48 (comparing these two processes). Not surprisingly, the PMA
process represents a much more significant financial barrier to the market ($111,000 to $828,000
per device) than the 510k process ($50 to $2,000 per device). See Lohr v. Medtronic, Inc., 

, 1345 n. 14 (11th Cir.1995) (citation omitted), aff'd in part & rev'd in part, 

, 

, 

(1996).
   2
    The FDA also regulates the testing of these devices by requiring manufacturers to apply for
an Investigational Device Exemption ("IDE"). The application for an IDE is itself fairly
extensive, and the FDA will not approve an IDE if there is reason to believe the device will be
ineffective or present unreasonable safety risks to patients. See 21 C.F.R. § 812.30(b)(4).

                                                 4
21 C.F.R. § 814.80. The FDA may withdraw its marketing approval if the manufacturer makes any

such changes without prior approval. See 21 U.S.C. § 360e(e)(1); 21 C.F.R. § 814.46(a)(2).3

B. The PMA Process for the 4004/M Lead

       The PMA process preceding the FDA's approval of Medtronic's 4004/M pacemaker lead was

an extensive one. In 1982, the FDA approved Medtronic's application for an IDE to conduct clinical

tests on a predecessor lead, the Model 4003 lead; Medtronic submitted the results of those trials to

the FDA when it filed a PMA application for the Model 4003. During that process, the FDA asked

Medtronic to submit information that addressed the effect of long-term degradation of the insulating

materials on the Model 4003 lead. In February 1984, Medtronic responded with studies and reports

that revealed that some of the leads experienced environmental stress cracking failures but supported

Medtronic's view that Pellethane 80-A polyurethane, the Model 4003 lead's insulating material, was

biostable and suitable for long-term implants. The FDA requested still further tests involving the

performance of similar leads with identical insulation materials and referred the Model 4003

application to an outside panel of experts, which concluded that Medtronic had provided the

requisite reasonable assurances of safety and effectiveness. The FDA approved the Model 4003

PMA application on July 29, 1986.

       On July 15, 1988, Medtronic filed a PMA application for the 4004/M as a supplement to the

Model 4003 PMA application. The supplemental PMA application relied on the information that

Medtronic already had submitted to the FDA and identified the lead's insulating material as

Pellethane 80-A. The supplemental PMA application also described Medtronic's research and testing



   3
   For a detailed description of the PMA process, see Worthy v. Collagen Corp., 

, 363-64 (Tex.), cert. denied, --- U.S. ----, 

, 

(1998).

                                                 5
on environmental stress cracking and metal-induced oxidation, both known as potential causes of

defects in leads that used polyurethane insulating material. On February 10, 1989, the FDA

approved the supplemental application for the 4004/M with an order that included a list of

"Conditions of Approval." Medtronic now seeks to use the FDA's approval to preempt Goodlin's

claims concerning the 4004/M lead.

II. Preemption Under the MDA

        By virtue of the Constitution's Supremacy Clause,4 it long has been settled that "state law that

conflicts with federal law is "without effect.' " Cipollone v. Liggett Group, Inc., 

, 516,

, 2617, 

(1992) (quoting Maryland v. Louisiana, 

, 746,

, 2128, 

(1981) and citing M'Culloch v. Maryland, 17 U.S. (4 Wheat.)

316, 427, 

(1819)). A federal statute may preempt state law either expressly, by the

statute's language, or implicitly, by the statute's structure and purpose. 

at 2617. In the

absence of an express command, federal law will preempt state law if that law actually conflicts with

federal law or if the federal law "so thoroughly occupies a legislative field as to make reasonable

the inference that Congress left no room for the States to supplement it." 

at 2617

(internal quotations and citations omitted).5

        The MDA contains an express provision that governs the extent to which the federal statute

preempts state law:


   4
   The Supremacy Clause provides that: "the Laws of the United States ... shall be the supreme
Law of the Land." U.S. Const., art. VI, cl. 2.
   5
    This latter form falls under the general heading of implied preemption. See generally Irving
v. Mazda Motor Corp., 

(11th Cir.), cert. denied, --- U.S. ----, 

, ---
L.Ed.2d---- (1998) (describing and applying the different forms of preemption). Although
Medtronic has raised an implied preemption argument, we find it to be without merit.

                                                   6
       (a) General rule

               Except as provided in subsection (b) of this section,6 no State or political subdivision
       of a State may establish or continue in effect with respect to a device intended for human use
       any requirement—

               (1) which is different from, or in addition to, any requirement applicable under this
               chapter to the device, and

               (2) which relates to the safety or effectiveness of the device or to any other matter
               included in a requirement applicable to the device under this chapter.

21 U.S.C. § 360k(a). The Supreme Court attempted to elucidate the extent to which section 360k(a)

preempts product liability suits arising under state law in Medtronic, Inc. v. Lohr, 

, 

, 

(1996), which involved a different allegedly defective Medtronic

pacemaker lead. Despite the striking superficial similarity of the cases, the Supreme Court's

disposition of Lohr provides little more than a rudimentary analytical framework to guide our

resolution of Medtronic's preemption claims in this case because Lohr involved the 510k process

rather than the PMA process, and because the Court fractured in an all but irreconcilable manner

over the extent to which section 360k(a) would ever preempt a general state common law tort claim.

See Mitchell v. Collagen Corp., 

, 910 (7th Cir.1997), cert. denied, --- U.S. ----, 

, 

(1998).7


   6
    Subsection (b) provides a means for a state or political subdivision thereof to apply for an
exemption to preemption when compelling local conditions require a more stringent
requirement. See 21 U.S.C. § 360k(b).
   7
    The Lohr Court split 4-4 over whether a jury's imposition of liability in a product liability
suit pursuant to state common law tort duties would ever amount to a conflicting state
requirement subject to federal preemption. Justice Breyer provided the fifth vote necessary to
support the Court's holding that none of the Lohrs' claims were preempted but asserted that he
agreed with Justice O'Connor's dissenting opinion on the extent to which more appropriate FDA
requirements might preempt state law claims. See 

, 116 S.Ct. at 2259
(Breyer, J., concurring). A number of courts have parsed these opinions and the actual votes

                                                  7
        Nevertheless, the Lohr Court instructed that two broad "presumptions about the nature of

pre-emption" inform the interpretation of section 360k(a). 

, 116 S.Ct. at 2250.

First, the Court explained that deference to state sovereignty, particularly in fields that the state

governments traditionally have occupied, requires an assumption that Congress will not supersede

"the historic police powers" of the states by federal statute without making that purpose "clear and

manifest." 

at 2250 (quoting Rice v. Santa Fe Elevator Corp., 

, 230, 

, 1152, 

(1947)). Second, the Court cautioned that " "[t]he purpose of

Congress is the ultimate touchstone' in every pre-emption case." 

at 2250 (quoting

Retail Clerks Int'l Ass'n Local 1625 v. Schermerhorn, 

, 103, 

, 223, 

(1963)). The MDA's preemption provision and its surrounding statutory framework,

therefore, provide our primary guide for discerning Congressional intent regarding the scope of

preemption, but we must also examine the "structure and purpose of the statute as a whole" by

reviewing the "way in which Congress intended the statute and its surrounding regulatory scheme

to affect business, consumers, and the law." 

116 S.Ct. at 2251 (internal quotation

omitted).

        In considering whether the MDA accords a federal obligation preemptive effect, the Lohr

Court read section 360k(a) to demand three things: (1) the imposition of a specific federal

requirement that (2) applied to a particular device and (3) focused on the safety and effectiveness



only to arrive at conflicting positions. Compare 

(noting that it would
have made little sense for Justice Breyer to write separately if he agreed that most state tort
claims were not preempted) with Oja v. Howmedica, Inc., 

, 789 (10th Cir.1997)
(finding no preemption of a general state common law tort claim by relying on Justice Breyer's
vote to concur in the judgment and ignoring the reasoning of his concurring opinion).
Fortunately, we need not enter that particular fray because we can resolve this case on the basis
of the federal requirement alone.

                                                 8
of the device. The Court held that the 510k process did not satisfy the preemption provision, in large

part, because the FDA's review addressed substantial equivalence rather than safety and

effectiveness. 

116 S.Ct. at 2254-55. The PMA process at issue in the case before us

addresses safety and effectiveness; indeed, the entire purpose of the PMA process is for the FDA

to obtain a "reasonable assurance" that the device is safe and effective. See 21 U.S.C. §

360c(a)(1)(C). Accordingly, we now turn to the question of whether the PMA process satisfies

section 360k(a)'s two other conditions by imposing any specific federal requirement on a particular

device.

          In addressing the federal requirement condition of section 360k(a)(1), the Lohr Court sought

guidance from an FDA regulation interpreting the preemption provision. The Court noted that the

language of section 360k(a) was unclear and that Congress expressly had given the FDA authority

to assess the preemptive effect of its own requirements on state laws. 

116 S.Ct. at

2255-56 (relying on 21 U.S.C. §§ 371(a) & 360k(b)). Although the Court may have avoided the

question of whether the FDA's regulations were due any deference under Chevron, U.S.A., Inc. v.

Natural Resources Defense Council, Inc., 

, 

, 

(1984), cf.

, 116 S.Ct. at 2263 (O'Connor, J., concurring in part and dissenting in part),

five Justices agreed that the FDA's "view of the statute" was entitled to "substantial weight." 

116 S.Ct. at 2256; see 

116 S.Ct. at 2260-61 (Breyer, J., concurring). The FDA's

regulation interpreting section 360k, issued in 1978, advises that:

          State or local requirements are preempted only when the [FDA] has established specific
          counterpart regulations or there are other specific requirements applicable to a particular
          device under the act, thereby making any existing divergent State or local requirements
          applicable to the device different from, or in addition to, the specific [FDA] requirements.

21 C.F.R. § 808.1(d).

                                                   9
       Considered together, section 360k(a)(1) grants preemptive effect to any federal "requirement

applicable under this chapter to the device," and the FDA regulation reads that language to include

only "specific counterpart regulations" or "specific requirements" that apply to "a particular device."

21 C.F.R. § 808.1(d). Accordingly, to prevail on its preemption argument in this case, Medtronic

must identify a specific federal requirement imposed on its particular device that would preempt any

conflicting or additional state requirement inherent in a jury verdict in Goodlin's favor. Medtronic

argues that the FDA's approval of its 4004/M lead, which required the FDA to find that Medtronic

had provided a reasonable assurance of the device's safety and effectiveness, amounts to the

imposition of such a requirement. Medtronic also cites the FDA's letter of approval and the attached

"Conditions of Approval," as well as the FDA's demand that Medtronic not alter the device in any

way affecting the safety or effectiveness of the 4004/M lead, as preempting requirements.8 We

address each argument in turn.

A. PMA Approval

        In this court's own review of Lohr, before the Supreme Court considered the case, we voiced

substantial doubt that the FDA's 510k approval process, which permits a successful applicant to

market its device, imposed a specific requirement upon the device. See Lohr v. Medtronic, Inc., 

(11th Cir.1995), aff'd in part & rev'd in part, 

, 

, 

    Medtronic also points out that in addition to compelling manufacturers to submit to the PMA
process, the MDA and the FDA's regulations specifically require manufacturers to provide
substantial relevant information and disclosures. We would have to consider the MDA's
provisions calling for PMA review of the type of medical device at issue in this case "specific
requirements," although it is not obvious that these requirements are device-specific, see infra
Part II(B). These requirements need not detain us, however, because the state of Florida has
passed no provisions that would conflict with the general PMA requirement by permitting
Medtronic to market the device in Florida without receiving FDA approval. We presume that
such efforts necessarily would have no effect in view of § 360k(a).

                                                  10
700 (1996). The majority of our discussion in support of our decision to deny the 510k process

preemptive effect addressed our primary concern that the process confines the FDA's consideration

to substantial equivalence rather than safety and effectiveness. 

Nevertheless, we

also expressed reservations about whether any finding pursuant to the 510k process would constitute

a specific federal requirement,9 and we made those misgivings part of our decision by holding that

the FDA's 510k approval, standing alone, "does not impose specific requirements on a device for

preemption purposes." 

        Similarly, when the Supreme Court considered the preemptive effect of a device's progress

through the 510k process, the Court focused its attention on the scope and focus of the 510k inquiry,

which are limited to substantial equivalence rather than safety and effectiveness. See Lohr, 518 U.S.

at 

. The Court's opinion,11 however, also refers to the panel's concern

that the 510k process "imposes no "requirement' " on the design of the pacemaker and the panel's

   9
   We wrote, "[e]ven assuming that a safety and effectiveness finding would constitute a
specific design requirement under the MDA, we are not convinced that 510(k) approval
constitutes a finding of safety and effectiveness." 

(emphasis added).
   10
     In another section of our Lohr opinion, in which we rejected the plaintiff's assertion that §
360k and the FDA's interpreting regulation contemplated a device-specific federal requirement,
we suggested that the PMA process was a much better candidate for preemption than the 510k
process because of its heightened rigor. 

& nn. 14 & 15. Given our subsequent
misgivings about converting the FDA's 510k approval into a specific requirement, however, we
cannot read this portion of our opinion to suggest that the PMA process is itself preemptive.
Instead, the Lohr panel used the PMA process as an example to support its view that the federal
requirement in § 360k(a)(1) need not be device-specific. Based on this understanding, the Lohr
panel held that the MDA's good manufacturing practices ("GMPs"), which apply generally to
almost all manufacturers of medical devices, were specific requirements and thus entitled to
preemptive effect. 

The Supreme Court, however, held that § 360k(a)(1) does
demand device-specificity and reversed the panel on this point. See 

,
116 S.Ct. at 2257-58.
   11
    The relevant discussion appears in section V of the plurality opinion, in which Justice
Breyer concurred. 

116 S.Ct. at 2261-62 (Breyer, J., concurring).

                                                 11
conclusion that "the requirements with which the company had to comply [as a consequence of 510k

review] were not sufficiently concrete to constitute a pre-empting federal requirement." 

116 S.Ct. at 2254. Moreover, the Court's analysis of the 510k process explains that the FDA's

finding of substantial equivalence "did not "require' Medtronics' pacemaker to take any particular

form for any particular reason." 

116 S.Ct. at 2254 (emphases added). Finally, the partial

dissenters, who would have found preemption elsewhere in the case far more readily than the

majority, concurred in this part of the opinion and rejected preemption as a consequence of surviving

the 510k process for both reasons: "Because the § 510(k) process seeks merely to establish whether

a pre-1976 device and a post-1976 device are equivalent, and places no "requirements' on a device,

the Lohrs' defective design claim is not pre-empted."12 

116 S.Ct. at 2264 (emphases

added); cf. 

116 S.Ct. at 2261 (Breyer, J., concurring) ("Insofar as there are any applicable

FDA requirements here, those requirements ... are not "specific' in any relevant sense."). See also

In re Orthopedic Bone Screw Prods. Liab. Litig., 

, 823 (3d Cir.1998) (stating that the

Lohr Court gave the 510k process no preemptive effect because it imposed no requirement).

        Accordingly, although the Lohr case had little to do with the PMA process, which differs in

significant ways from the 510k process at issue there, at least eight, and probably all nine, of the

otherwise divided Justices expressed reservations as to whether the FDA's 510k review process and


   12
     Of these two bases for deciding that the 510k process has no preemptive effect, the latter
finds far more support in the language of § 360k(a). That section provides that no state may
establish a requirement that (1) is different from a federal requirement and (2) relates to safety
and effectiveness. Section 360k(a)(1) contemplates a federal requirement, which the FDA reads
to mean a specific requirement. See 21 C.F.R. § 808.1(d). Section 360k(a)(2) demands that the
requirement relate to safety and effectiveness, but it is at least ambiguous whether § 360k(a)(2)
modifies the state or federal requirement at issue. The Supreme Court plainly read the provision
to apply to the federal requirement, but an argument could be made that the more natural reading
of the provision is as a limitation on the state requirement.

                                                  12
approval, standing alone, imposed any "requirement" on a device. See Worthy v. Collagen Corp.,

, 369-70 (Tex.1998), cert. denied, --- U.S. ----, 

, 

(1998)(explaining that the Supreme Court's decision that the 510k process was "too general to have

preemptive effect" was unanimous). As noted above, because the PMA process before us focuses

on safety and effectiveness, we must examine these misgivings further to determine whether the

FDA's PMA process, which produces a finding that the manufacturer has provided the reasonable

assurances of safety and effectiveness necessary to market the device, translates into the necessary

imposition of a "specific requirement."

        Our initial concern with this question is a conceptual one. Absent a more specific statutory

definition, we must accord the language at issue its ordinary meaning. See, e.g., Park "N Fly, Inc.

v. Dollar Park and Fly, Inc., 

, 194, 

, 661, 

(1985)("Statutory construction must begin with the language employed by Congress and the

assumption that the ordinary meaning of that language accurately expresses the legislative

purpose."). We also may consider Congress's use of a particular term elsewhere in the statute to

determine its proper meaning within the context of the statutory scheme. See, e.g., Estate of Cowart

v. Nicklos Drilling Co., 

, 479, 

, 2596, 

(1992). In

ordinary usage, a requirement refers to "something that is wanted or needed" or "something called

for or demanded: a requisite or essential condition." Webster's Third New Int'l Dictionary 1929

(1986) (emphases added). Similarly, within section 360k, Congress referred to a requirement as

something a state or political subdivision could "establish," which appears to contemplate the state's

creation of and, thus, identification of some thing. 21 U.S.C. § 360k(a). Finally, the FDA's

interpretive regulation, which describes the federal requirement as "specific counterpart regulations"


                                                 13
that the FDA "has established," or "specific requirements" that apply to the device under the MDA,

21 C.F.R. § 808.1(d), also indicates that a section 360k(a) preempting federal requirement must be

some ascertainable condition.13 The ordinary construction of the language of section 360k, as well

as the use of the term "requirement" in the broader statutory context and its interpretation in the

FDA's regulation, therefore, all contemplate the imposition of some identifiable precondition that

applies to the device in question. Indeed, the statute, the FDA's regulation, and the Supreme Court's

analysis in Lohr instruct us to conduct a "careful comparison" between the state and federal

requirements at issue. 

, 116 S.Ct. at 2257-58. Such a comparison is

impossible if we cannot identify or ascertain the precise federal requirement at issue. Our

conceptual difficulty with Medtronic's argument stems from our inability to ascertain any such

identifiable requirement from the FDA's approval of Medtronic's 4004/M lead.

        Medtronic points out that even a cursory review of the statutory framework reveals that the

MDA imposes a legion of readily identifiable requirements upon the PMA applicant. See 

Part I(A); 

(providing an overview). Despite the specificity

and considerable rigor of these conditions, see supra note 8, however, neither the FDA's actual

review of a device and its supporting information nor the agency's eventual approval of the device

imposes any ascertainable requirement upon the device. In the typical PMA review and approval

and, more particularly, in the context of the 4004/M PMA, the FDA issues no regulation, order, or



   13
    The FDA's interpretive regulation also speaks of the conflicting state regulation in terms that
contemplate an ascertainable condition that the state must establish in one manner or another.
See 21 C.F.R. § 808.1(b) (explaining that federal law preempts requirements "having the force
and effect of law (whether established by statute, ordinance, regulation or court decision).").
Furthermore, the FDA's description of state requirements in the remainder of the interpretive
regulation refers only to concrete and identifiable rules and regulations. 

808.1(d)(1-10).

                                                 14
any other statement of its substantive benchmark. Cf. Papike v. Tambrands Inc., 

, 740-

41 (9th Cir.), cert. denied, --- U.S. ----, 

, 

(1997) (finding preemption

based on an ascertainable requirement in an express FDA regulation requiring specific warnings on

a device's packaging); 

n. 

n. 9 (plurality opinion) ("In the

MDA, no ... specifics exist until the FDA provides them."). The approval represents only a finding

that the manufacturer's proposal to market a device has reasonably assured the FDA of the device's

safety and effectiveness. Nor does the FDA's willingness to notify an applicant of deficiencies and

to propose modifications to the PMA application add any further force to Medtronic's argument for

preemption, because an applicant who corrects or modifies a deficient PMA application before

receiving the FDA's approval stands in no better position than an applicant whose initial PMA

application was flawless.14 In either case, the FDA enters a finding that the applicant has furnished

the relevant assurances and therefore may begin to market its device. In neither case, however, does

the approval provide any indication of what (if any) specific substantive requirements the FDA may

have applied to reach that result.15 Compare Hurley v. Lederle Lab. Div. of Am. Cyanamid Co., 863


   14
     In this vein, Medtronic argues that the FDA imposed a number of specific requirements on
the 4004/M during the process of reviewing the PMA application. Our review of the record,
however, reveals that these requirements amounted to nothing more than requests for further
information and explanations of data already before the FDA. These requests for information
may shed light upon the issues the FDA examined but do not impose any specific requirement
upon the device. We also note that the Lohr Court did not consider the FDA's power to make
similar requests for additional information during the 510k review, see 21 C.F.R. § 807.87(l ), as
a factor that would support according that process preemptive effect.
   15
     In 1997, the FDA promulgated a proposed rule on the preemption of state product liability
claims under the MDA. See 62 Fed.Reg. 65,384 (1997). In that proposed rule, the FDA's
analysis of its general approval processes (the 510k, the IDE, and the PMA) echoed our concern
regarding the imposition of an ascertainable "specific requirement" as contemplated in §
360k(a)(1). 

As a result of irregularities in the timing and circumstances of the
FDA's action and in response to Congressional criticism of those circumstances, however, the

                                                 

, 1177 (5th Cir.1988) (explaining that the FDA's approval of a certain form of vaccine

provides "no basis for finding a federal interest in" that form) with 

, 116 S.Ct.

at 2257 ("[P]re-emption [must] occur only where a particular state requirement threatens to interfere

with a specific federal interest.") (emphasis added).

        Medtronic seeks to convert the FDA's finding and the accompanying permission to market

its device into the federal government's implied validation of the safety of its device and every step

of its manufacture and, then, to use that validation as a shield against liability in tort. The FDA's

approval is clearly specific to the device under review, but because the approval itself neither reveals

nor imposes any ascertainable substantive prerequisite for approval that we could compare to a

purportedly conflicting state requirement, the approval itself does not fit within section 360k(a)(1)'s

demand for a specific federal requirement. As the New York Appellate Division persuasively

explained, "while a PMA review is considerably more rigorous and detailed than the premarket

notification [510k] process at issue in [Lohr v.] Medtronic, it is, in fact, no more "specific' a




FDA withdrew the proposed rule in July 1998. See 63 Fed.Reg. 39,789 (1998). Accordingly,
we have given the FDA's expression of its views in this proposed rule no authoritative weight or
deference. Nor do we defer to any position the FDA may have taken as an amicus curiae in
cases involving issues of preemption. See McKee v. Sullivan, 

, 1439 n. 3 (11th
Cir.1990) ("[E]vidence of a litigating position is insufficient to establish an agency's
interpretation.").

                Nevertheless, we find the analysis of the PMA process presented in the FDA's
        proposed rule interesting for two reasons. First, we are convinced that the proposed
        rule's analysis is faithful to the language of § 360k(a)(1), the broader statutory
        framework, and Congress's purpose in passing the MDA. Second, we find it unsettling
        that the agency charged with conducting PMA review has doubts regarding whether an
        approval pursuant to that process should preclude subsequent state tort liability.

                                                  16
requirement."    Sowell v. Bausch & Lomb, Inc., 

, 

, 20

(N.Y.App.Div.1997).16

B. The FDA's Conditions of Approval

        Medtronic also points to the "Conditions of Approval" that accompanied the FDA's approval

of the PMA application for the 4004/M lead, as well as the agency's demand that Medtronic make

no changes to the device without first seeking FDA approval, as possible sources for a preempting

federal requirement.    Although we agree that these conditions constitute specific federal

requirements, as discussed in part II(A) above, we are not convinced that these requirements satisfy

section 360k(a)(1)'s further admonition that a preempting requirement be "applicable under this

chapter to the device." 21 U.S.C. § 360k(a)(1).


   16
     Medtronic argues that our adoption of Slater v. Optical Radiation Corp., 

(7th
Cir.1992) in Duncan v. Iolab Corp., 

, 195 (11th Cir.1994) precludes our analysis and
conclusions here. Slater, however, involved the preemptive effect of the IDE process, not the
PMA process, and therefore does not control our disposition of this case. Moreover, Slater
explicitly relied on the experimental nature of the device undergoing IDE review. See 

.

                 Nevertheless, we acknowledge that part of the reasoning in Slater is at odds with
        our analysis today because the Slater court implied a specific federal requirement from
        the FDA's determination that the device was sufficiently safe and effective to permit
        experimental use. 

analysis, in section II(A), of the manner in which the
        Supreme Court addressed section 360k(a)(1)'s demand for a specific federal requirement
        in its intervening Lohr decision, however, we do not believe that Slater 's reasoning on
        this point has survived. See Niehoff v. Surgidev Corp., 

, 819-20
        (Ky.1997), cert. denied, --- U.S. ----, 

, 

(1998) (rejecting
        Slater in light of the Supreme Court's demand for a specific federal requirement). On this
        point, we part company with the Seventh Circuit, which continues to apply the relevant
        portion of Slater despite Lohr. See Mitchell v. Collagen Corp., 

, 911 (7th
        Cir.1997) (applying Slater 's approach without citing the case); Chambers v. Osteonics
        Corp., 

, 1246-47 (7th Cir.1997)(relying on the case explicitly). In any
        event, to the extent Slater is at odds with our decision today, we believe the Supreme
        Court's reasoning in Lohr calls that case, and thus our adoption of it in Duncan, into
        question.

                                                  17
       The MDA permits the FDA to impose similar conditions on devices it approves pursuant to

the 510k process. See, e.g., 21 U.S.C. § 360j(e) (giving the FDA the authority to impose conditions

on the sale of any device); cf. 

(referring to the FDA's existing authority to enforce

restrictions on the sale or distribution "of a device that are part of a determination of substantial

equivalence, established as a condition of approval, or promulgated through regulations").

Moreover, the Supreme Court in Lohr took note of these conditions and the FDA's "continuing

authority to exclude the device from the market if its design is changed" and recited Medtronic's

arguments in favor of construing these factors as preemptive requirements. Lohr, 518 U.S. at 

; see also 21 C.F.R. § 807.81(a)(3) (requiring premarket notification for the

reintroduction into commercial distribution of any device that is about to be significantly changed

or modified). Nevertheless, the Court found these arguments insufficient to fit the 510k approval

process within the confines of section 360k(a)(1) and declined to grant the 510k process preemptive

effect. See Part 

.

       More significantly, the Lohr Court construed section 360k(a)(1)'s description of a federal

requirement "applicable under this chapter to the device" as an instruction to limit preemption to

device-specific requirements. To interpret the relevant language, the Court again relied on the

FDA's interpreting regulation, which reads section 360k(a)(1) to demand a specific federal

requirement "applicable to a particular device." 21 C.F.R. § 808.1(d) (emphasis added), quoted in

, 116 S.Ct. at 2257. The Court then noted the FDA's "overarching concern"

regarding a broader construction of preemption and determined that the FDA's general labeling

requirements and its Good Manufacturing Practices ("GMPs") were too general to merit preemptive

effect under the statute and regulation. See 

, 116 S.Ct. at 2256-58. A


                                                 18
similar concern animates the Court's discussion of the general nature of the conditions the FDA

imposed in its letter notifying Medtronic of its approval of the device pursuant to the 510k process.

116 S.Ct. at 2254 ("That letter only required Medtronic to comply with "general

standards'—the lowest level of protection "applicable to all medical devices'....").

           Analogously, the restrictions Medtronic proffers in this case are entirely general in nature,

and the FDA has not promulgated them with respect to the "particular device" before us, the

4004/M, or even with respect to the class of specific devices at issue, pacemaker leads. The

"Conditions of Approval" document enclosed with the letter that noted the FDA's approval of the

4004/M PMA application sets forth rules and regulations generally applicable to all devices

approved through the PMA process. For example, the "Conditions of Approval" remind Medtronic

of its obligation to provide post-approval reports, to refrain from changing the device without FDA

approval, and to report adverse reactions and device defects.17 The document, dated almost two

years before Medtronic submitted its supplemental PMA application, is cast in the most generic of

terms and mentions neither the 4004/M nor even pacemaker leads as a class of devices.18 As the

Supreme Court explained:

           [T]he federal requirements reflect important but entirely generic concerns about device
           regulation generally, not the sort of concerns regarding a specific device or field of device
           regulation which the statute or regulations were designed to protect from potentially
           contradictory state requirements.

, 116 S.Ct. at 2258. We do not believe that requirements applicable to all

devices that receive the FDA's approval via the PMA process satisfy the Court's demand for a



   17
        See R1-24, Ex. E-3.
   18
        

3.

                                                    19
specific requirement that applies to a particular device. See Kennedy v. Collagen Corp., 

, 1458-59 (9th Cir.1995) (pre-Lohr case expressing doubt that Class III devices collectively

constitute a "particular device" within the meaning of section 360k(a)(1) and the FDA's interpreting

regulation), overruled in part on other grounds by Lohr, 

, 

, 

.

C. The "Ultimate Touchstone" of Congressional Intent

        We recognize that our conclusions on these questions, although not without precedent,19 are

at odds with the results reached in a number of cases both before and after the Supreme Court's

decision in Lohr. See Mitchell v. Collagen Corp., 

, 911 & n. 2 (7th Cir.1997) (finding

that PMA approval constitutes a specific federal regulation and examining cases both in support and

to the contrary); 

(surveying cases before and after Lohr ).

Nevertheless, we remain convinced that our conceptual difficulty with Medtronic's attempts to

divine a specific federal requirement from the FDA's approval of its PMA application reflects the

real difference between the questions at stake during the PMA process and the discrete issues

presented in a product liability suit.20 The PMA process permits the FDA to regulate the


   19
    See 

(pre-Lohr case finding that the PMA process imposes no
specific federal requirement), overruled in part on other grounds by Lohr, 

, 

, 

; Lakie v. SmithKline Beecham, 

, 54 (D.D.C.1997)
("The fact that the PMA process requires certain information and mandates certain procedures
from manufacturers does not transform the PMA process itself into a specific federal requirement
which triggers preemption and protects a manufacturer from suit."); accord 

; Walker v. Johnson & Johnson Vision Prods., Inc., 217 Mich.App. 705, 

(Mich.App.1996).
   20
     We recognize that our decision may have implications beyond the preemption of state tort
suits. Our analysis of the PMA review process and our decision that the FDA's approval
imposes no preemptive requirement might preclude the express preemption of any conflicting
state requirement, no matter how the state asserts it. Although we find it difficult to conceive of

                                                20
introduction and sale of medical devices to assure their minimal safety for public consumption—it

does not appear to address the appropriate standards of liability once the product enters the

marketplace. Our inability to discern a specific requirement that fits the demands of section 360k(a)

in the FDA's approval process, therefore, finds broader support in the language and structure of the

MDA and is consistent with the factual backdrop that prompted Congress to enact the MDA.

        Neither the MDA itself nor the FDA's interpretive regulations directly addresses the question

of liability arising in connection with defective medical devices. Instead, the preamble to the MDA

states that the amendments are for the purpose of "provid[ing] for the safety and effectiveness of

medical devices intended for human use." Pub.L. No. 94-295, 90 Stat. 539, 539 (1976) (preamble).

Similarly, the legislative history of the MDA fails to address issues of liability for defective devices.

See 

, 116 S.Ct. at 2253 (plurality opinion). Instead, the legislative history

recounts the difficulty the FDA experienced in its earlier attempts to keep dangerous medical

devices out of the marketplace. See S.Rep. No. 94-33 at 2-7 (1976), reprinted in 1976 U.S.C.C.A.N.

1070, 1071-76. This attention to the regulation of medical devices before they reach the marketplace

is consistent with the events that prompted Congress to consider the MDA. As the Supreme Court

observed in Lohr, several highly publicized incidents involving defective medical devices,




any such hypothetical state requirement that actually would conflict with the FDA's approval
rather than the federal laws preventing the sale of unapproved devices, see supra note 8, we note
the Supreme Court's recent teaching that the presence of an express preemption provision in a
federal statute does not preclude field or conflict preemption. See Freightliner Corp. v. Myrick,

, 

, 

(1995), cited in 

, 116 S.Ct.
at 2259 (plurality opinion). To the extent, therefore, that a state's law " "stands as an obstacle to
the accomplishment and execution of the full purposes and objectives of Congress' " as
embodied in the PMA approval process, the state's efforts still may fall to preemption.
Freightliner 

, 115 S.Ct. at 1487 (quoting Hines v. Davidowitz, 

, 67, 

, 404, 

(1941)).

                                                   21
particularly the Dalkon Shield intrauterine device, gave rise to Congress's legislation in this area.

See 

, 116 S.Ct. at 2246. It would have been inconsistent for the same

Congress that enacted these sweeping reforms, intending to make a potentially dangerous industry

safer for patients by blocking the admission of defective devices to the market, then to preempt

product liability suits when those devices caused injury. Moreover, we find no support for

Medtronic's assertions that a concern for preserving innovation prompted Congress even to consider,

let alone enact, preemption of tort liability in all cases involving devices that survived the PMA

process. 

116 S.Ct. at 2253 (plurality opinion). Instead it appears that the members

of Congress who sought to foster continued innovation in the field focused their efforts on reducing

the regulatory burden that manufacturers would have to bear before they could market their

products. 

(plurality opinion). Again, these efforts are consistent with our

observation that Congress intended to regulate medical devices before they reached consumers,

rather than address their consequences once on the market.

       Other provisions of the statutory scheme also indicate that Congress expected some state tort

liability to survive the MDA. For example, the statute contains a savings clause that specifically

addresses the MDA's effect on other liabilities arising from defective medical devices: "Compliance

with an order issued under this section shall not relieve any person from liability under Federal or

State law." 21 U.S.C. § 360h(d). The effect of this savings clause is somewhat ambiguous because

it appears in a section that addresses the FDA's powers to provide notification and other remedies

when the agency discovers that a medical device (presumably including one that received PMA

approval) presents an "unreasonable risk of substantial harm to the public health." 

As a matter of careful statutory construction, therefore, we would have to read section 360h(d) to


                                                 22
refer only to compliance with FDA orders regarding notification, repair, replacement, refund, or

reimbursement—and not to include compliance with the PMA process, which arises under a

different section of the MDA. This limitation on section 360h(d)'s technical application, however,

need not compel us to ignore the provision's broader implications because product liability in tort

is the most immediately obvious source of state law liability that ordinarily would arise in a situation

implicating the FDA's section 360h authority. Moreover, although the Lohr panel refused to read

section 360h(d) as a vehicle to reject all preemption under the MDA because that section does not

speak to the type of state liability contemplated and because a general savings clause cannot

supersede a more specific preemption provision, see 

, rev'd in part and

aff'd. in part, 

, 

, 

, the Supreme Court never addressed

the impact of section 360h(d) on its preemption analysis. Despite these lingering concerns, we

would misread neither the plain language of section 360h(d) nor the Lohr panel's interpretation of

the law by concluding that the savings clause casts real doubt on the idea that Congress intended to

preempt state tort liability for all PMA approved devices. Cf. Irving v. Mazda Motor Corp., 

, 767-68 (11th Cir.1998) (holding that a federal regulatory statute that includes a

preemption clause and a savings clause is ambiguous on the preemption of state common law

claims).

        Finally, and as the Lohr plurality observed, the MDA provides no federal means by which

injured plaintiffs can pursue legal remedies against the manufacturers of defective medical devices.

See 

, 116 S.Ct. at 2251 (plurality opinion)("[T]here is no explicit private cause

of action against manufacturers contained in the MDA, and no suggestion that the Act created an

implied private right of action....").    Reading the PMA process to impose specific federal


                                                  23
requirements that enjoy preemptive effect under section 360k, therefore, would deprive all persons

suffering injury as a result of a defective device—the very class of persons that Congress intended

to protect by enacting the MDA—of "most, if not all relief." Id. at 

(plurality

opinion). The Supreme Court considered an analogous situation in Silkwood v. Kerr-McGee Corp.,

, 

, 

(1984). In that case, Congress had enacted the Atomic

Energy Act (the "AEA") "to prohibit the States from regulating the safety aspects of nuclear

development," on the premise that the federal government's commission was more qualified to

define the safety standards that should control the industry. 

104 S.Ct. at 622. To support

its conclusion that the statute did not preempt state tort remedies and punitive damage awards

against the nuclear power industry, the Court observed that Congress had provided no indication that

it even had considered preempting state tort law liability. 

104 S.Ct. at 623. Moreover,

the Court refused to attribute any intent to preempt state tort claims after observing that preemption

would leave the public—the target of Congress's safety concerns—without a remedy, because

Congress had not enacted a federal private cause of action for injured plaintiffs: "It is difficult to

believe that Congress would, without comment, remove all means of judicial recourse for those

injured by illegal conduct." 

at 623, quoted in 

, 116 S.Ct. at 2251

(plurality opinion). We too are reluctant to conclude that Congress sought to remove all remedies

available to the very class of persons that it sought to protect when it enacted the MDA.

       In its attempts to discern Congress's intentions regarding the preemption of tort liability, the

Silkwood Court also looked to Congress's subsequent legislation in the field. The Court observed

that Congress had passed the Price-Anderson Act to provide a federal indemnification regime to

encourage private companies to enter the nuclear power industry despite the risk of significant state


                                                 24
tort liability. See Silkwood, 464 U.S. at 

. Although the indemnification

provisions had no application to the case at hand, the Court explained that their very existence

demonstrated that Congress never intended to preempt state tort remedies when it passed the AEA.

104 S.Ct. at 623-25. We find similar evidence of Congress's intent with regard to the

MDA in its 1994 attempt, albeit failed, to enact the Product Liability Fairness Act ("PLFA"). The

proposed act, which sought to create federal standards of product liability,21 would have prevented

private litigants from recovering punitive damages from the manufacturers of medical devices in

cases where the "drug or device" that caused a plaintiff's harm "was subject to pre-market approval

by the [FDA] with respect to the safety of the formulation or performance of the aspect of such drug

or device which caused the claimant's harm...." S. 687, 103d Cong. § 203 (1994). Although the bill

never became law, section 203's attempt to prevent plaintiffs suing the manufacturers of PMA

devices under state tort law (to the extent not inconsistent with the proposed federal standard) from

recovering punitive damages is significant because, if the 1976 Congress truly had intended section

360k(a) of the MDA to preempt all or most state law claims involving PMA approved devices, then

there would have been no need for the 1994 Congress to include those devices in its proposed

solution to the more general travails of product liability law.

        These factors indicate beyond any doubt that, at least with respect to the FDA's PMA

authority, Congress was deeply concerned with assuring the minimal safety of medical devices that



   21
    The PLFA would not have created a new federal cause of action but rather would have
imposed uniform standards of liability for product manufacturers and sellers. See S. 687, 103d
Cong. § 202. The proposed law would have permitted plaintiffs to bring causes of action
pursuant to applicable state law, to the extent not in conflict with the PFLA's provisions. 

Similarly, a plaintiff could also pursue punitive damages under "applicable law" to the
extent not in conflict with the PFLA. 

                                                 25
enter the marketplace but gave no appreciable thought to the effect such regulation should have on

any liability that might result from the sale and use of such medical devices. As a result, the PMA

process is proactive rather than reactive; it concerns the manufacturers' ability to market minimally

safe devices but makes no attempt to announce substantive safety standards that might determine

the outcome of a product liability suit. See S.Rep. No. 94-33 at 2 (1976), reprinted in 1976

U.S.C.C.A.N. 1070, 1071 ("Medical device legislation is intended to assure that medical devices ...

meet the requirements of safety and effectiveness before they are put in widespread use throughout

the United States.")(emphasis added). This view of the statutory scheme and the purposes behind

the MDA is in harmony with our reading of section 360k(a)(1)'s limitation on the type of specific

federal requirements to which Congress intended to grant preemptive effect and with our conceptual

objection to conjuring such specific federal requirements from the FDA's approval of particular

devices.

       Nevertheless, we can conceive of a situation in which Congress may have intended to

establish an exemption from state tort liability as a trade-off for imposing the PMA system upon new

medical devices. Congress would have been aware of such litigation given the backdrop of high

profile cases involving defective medical devices, and that experience could have led Congress to

substitute regulation for litigation by preempting all claims involving devices that received PMA

approval. Indeed, Congress recently attempted an ambitious, but more limited, attempt to make such

a trade-off by enacting the proposed Universal Tobacco Settlement Act and thereby bring a

negotiated resolution to years of tobacco litigation. See S. 1415, 105th Cong. (May 14, 1998).

Congress's controversial and ultimately unsuccessful experience with this particular attempt to

provide even limited immunity from suits arising under state product liability laws, however, only


                                                 26
bolsters our conviction that the 1976 Congress contemplated no such consequences under the

MDA.22 It is difficult to believe that Congress struck a similar bargain—regulation in exchange for

immunity from state tort suits—in the area of medical devices without mentioning its aspirations in

the statute or its legislative history and with nary a comment in the FDA's interpretive regulations

or in the contemporary reviews of industry observers. See 

& n. 

& n. 13 (plurality opinion).

        Finally, we are loath to infer a tacit trade-off between regulation and liability when it appears

that even the regulated industry was unaware of the purported bargain until relatively late in the day.

Our research reveals that the first reported decisions on the industry's attempts to assert federal

preemption of state product liability claims for devices subject to the FDA's approval regimes did

not appear until 1991, fifteen years after Congress passed the MDA. See Slater v. Optical Radiation

Corp., 

(N.D.Ill.1991), aff'd, 

, 1331 (7th Cir.1992) (recognizing that

the preemptive effect of an FDA issued IDE presented a matter of first impression at the appellate

level). We recognize that the costs and delays associated with the PMA process have led the

industry to avoid it when possible. See 

, 116 S. Ct at 2248 (noting that in 1990

eighty percent of new medical devices had entered the market without undergoing PMA review).



   22
     We note that the 1998 Congress that considered granting a number of domestic tobacco
companies immunity against state-initiated litigation and class actions (but not private,
individual lawsuits) did so directly and unambiguously. See S. 1415, 105th Cong. §§ 701-703.
We further observe that Congress rigorously defined this immunity in the proposed statute, 

it also planned to subject new tobacco products to FDA regulation and review
through a process akin to the MDA's PMA process, 

Finally, we observe that the
debate over granting even this limited immunity to tobacco manufacturers, and the price
Congress properly should have demanded for it, were matters of extreme and extended
controversy. Moreover, the FDA's concurrent attempts to regulate nicotine as a drug prompted a
blizzard of commentary from the legal academy and industry observers.

                                                   27
Even so, it seems unlikely that the industry would have ignored its immunity under the MDA for

so long after the statute's enactment if Congress, in fact, had intended to provide immunity in 1976.

       Just beneath the surface of Medtronic's arguments in support of preemption lies a relatively

appealing policy argument in favor of immunity for devices that receive the FDA's most extensive

review and approval. It seems presumptuous, to say the least, to permit a jury composed of ordinary

citizens, none of whom we can expect to have significant medical training, to second-guess a

decision, already extensively and rigorously considered by some of the most qualified minds in the

relevant medical and scientific fields, regarding the rather complicated question of the safety of a

particular medical device. As Medtronic described the PMA process for the 4004/M lead, a number

of government and independent experts, as well as Medtronic's own scientists, examined, over

several years, the performance of the Pellethane 80-A polyurethane insulating material at issue in

Goodlin's complaint and came to the conclusion that Medtronic had reasonably assured its safety.

Goodlin's complaint, however, demands that a jury—a much less scientifically qualified

body—decide whether the 4004/M lead was unreasonably dangerous because it used the Pellethane

80-A insulating material and, if so, to award damages.

       No matter how compelling we might find Medtronic's policy objections as citizens, as

judges, bound to apply the law rather than create it, we may not act on those objections here. The

jury system, although imperfect, is the method by which we resolve an ever-increasing number of

disputes, many of which might more appropriately be resolved by experts. We cannot accept that

Congress intended to exempt the manufacturers of medical devices from tort liability for all devices

subject to the PMA process on the scant evidence presented here. We also read the Supreme Court's

most recent admonition that "[t]he purpose of Congress is the ultimate touchstone in every


                                                 28
pre-emption case," 

, 116 S.Ct. at 2250 (internal quotation omitted), and the

Court's instruction that deference to state sovereignty requires us to assume that Congress does not

preempt the states' "historic police powers" without making its purpose "clear and manifest," 

at 2250 (internal quotation and citations omitted), as unmistakable directions that lead us to

today's decision. Accordingly, we may not bend the language of section 360k(a)(1) to permit the

manufacturers of medical devices to infer from the FDA's approval of a PMA application specific

federal requirements that remain unstated and unascertainable until an injured consumer brings a

lawsuit alleging a defect.

        Our decision does not mean that Medtronic's efforts to provide the FDA with reasonable

assurances regarding the 4004/M lead's safety and effectiveness have no bearing on the question of

its liability on Goodlin's claims. To the contrary, to prevail at trial, Goodlin must show either that

Medtronic designed the lead negligently or that the lead was inherently dangerous because the risks

it imposed outweighed its benefits.23 Medtronic's efforts to improve its product and the information

it collected in support of its safety will be relevant to these questions. The FDA's approval of the

device, particularly after an independent panel of experts recommended that approval, should

impress the jury that must evaluate the reasonableness of Medtronic's actions at the time it

manufactured and marketed the 4004/M lead. Although the task of presenting this information in

a manner that a jury can understand may make for a lengthy and complicated trial—and may even

demand a better solution—section 360k(a) of the MDA provides no means to avoid it.

                                          CONCLUSION


   23
     Goodlin also will have to prove that Medtronic's negligence or the device's inherent danger
caused her harm. As the district court observed, but did not decide, Goodlin's case faces some
serious causation problems under Florida law.

                                                 29
       We conclude that the FDA's approval of a medical device pursuant to the PMA process,

standing alone, imposes no specific federal requirement applicable to a particular device and,

therefore, has no preemptive effect under section 360k(a) of the MDA. Accordingly, we REVERSE

the district court's entry of summary judgment in Medtronic's favor and REMAND the case for

further proceedings consistent with this opinion.




                                                30