4th Circuit Asked To Rehear Whether 510(k) Evidence Belongs In Pelvic Mesh Trial

(February 14, 2017, 8:09 AM EST) -- RICHMOND, Va. — Ethicon Inc. and parent company Johnson & Johnson on Feb. 9 petitioned the Fourth Circuit U.S. Court of Appeals to grant an en banc rehearing on the issue whether any evidence about Food and Drug Administration dealings with 510(k)-cleared medical devices is admissible in a product liability case (Jo Huskey, et al. v. Ethicon, Inc., et al., No. 15-2118, 4th Cir.)....

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