| dbo:abstract
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- Riegel v. Medtronic, Inc., 552 U.S. 312 (2008), is a United States Supreme Court case in which the Court held that the pre-emption clause of the bars state common-law claims that challenge the effectiveness or safety of a medical device marketed in a form that received premarket approval from the Food and Drug Administration. It modified the rule in Medtronic, Inc. v. Lohr. (en)
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- 2451 (xsd:nonNegativeInteger)
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- 0001-12-04 (xsd:gMonthDay)
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- Riegel v. Medtronic, Inc., (en)
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- 0001-02-20 (xsd:gMonthDay)
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- Charles R. Riegel, et ux. v. Medtronic, Inc. (en)
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| dbp:holding
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- The MDA’s pre-emption clause bars common-law claims challenging the safety or effectiveness of a medical device marketed in a form that received premarket approval from the FDA. (en)
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| dbp:joinmajority
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- Roberts, Kennedy, Souter, Thomas, Breyer, Alito; Stevens (en)
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| dbp:justia
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| dbp:litigants
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- Riegel v. Medtronic, Inc. (en)
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| rdfs:comment
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- Riegel v. Medtronic, Inc., 552 U.S. 312 (2008), is a United States Supreme Court case in which the Court held that the pre-emption clause of the bars state common-law claims that challenge the effectiveness or safety of a medical device marketed in a form that received premarket approval from the Food and Drug Administration. It modified the rule in Medtronic, Inc. v. Lohr. (en)
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- Riegel v. Medtronic, Inc. (en)
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- (en)
- Charles R. Riegel, et ux. v. Medtronic, Inc. (en)
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