FDA 510(k) Applications Submitted by Synthes (USA) Products LLC/DePuy Orthopaedics Inc

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
K180310	02/05/2018	DePuy Synthes Trauma Orthopedic Plates and Screws	Synthes (USA) Products LLC/DePuy Orthopaedics Inc
K172975	09/27/2017	DePuy Synthes (USA) 5.0mm / 7.3mm Crimp Positioning Pins û MR Conditional, DePuy Synthes Variable Angle Positioning Pins û MR Conditional, DePuy Synthes Wire Mount û MR Conditional, DePuy Synthes Cerclage Positioning Pin û MR Conditional	Synthes (USA) Products LLC/DePuy Orthopaedics Inc