FDA 510(k) Applications Submitted by ELIZABETH JACOBS

FDA 510(k) Number Submission Date Device Name Applicant
K160553 02/29/2016 DePuy Synthes 4.0 mm and 5.0 mm Locking Screws û MR Conditional, DePuy Synthes Wrist Fusion Plate (WFP) û MR Conditional, DePuy Synthes Large Fragment Dynamic Compression Locking (DCL) System ûMR Conditional, DePuy Synthes Small Fragment Dynamic Compressi SYNTHES (USA) PRODUCTS LLC/DEPUY ORTHOPAEDICS INC
K182783 10/01/2018 DePuy Synthes Trauma Orthopedic Nail Implants DePuy Synthes


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