A-20/21/22/23-21 Elizabeth Hrymoc v. Ethicon, Inc. (085547)
Among other issues, in these product liability trials should defendants have been permitted to present evidence that they had obtained "Section 510(k) clearance" from the Food and Drug Administration for their pelvic mesh medical devices?
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A-20/21/22/23-21
- Certification granted : Oct. 22, 2021
- Posted: Oct. 22, 2021
- Argued: Feb. 27, 2023
- Decided: July 25, 2023