FDA 510(k) Applications Submitted by SYNTHES (USA) PRODUCTS, LLC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K172157	07/18/2017	DePuy Synthes Femoral Recon Nail System	Synthes (USA) Products, LLC
K160167	01/27/2016	DePuy Synthes TFNA Augmentation System	Synthes (USA) Products, LLC
K170802	03/17/2017	TRAUMACEMÖ V+ Injectable Bone Cement	Synthes (USA) Products, LLC
K131548	05/30/2013	SYNTHES TROCHANTERIC FIXATION NAIL - ADVANCED SYSTEM	SYNTHES (USA) PRODUCTS, LLC
K150099	01/20/2015	Depuy Synthes Variable Angle Locking Hand System (1.3 mm and 2.0 mm Plates and Screws)	SYNTHES (USA) PRODUCTS, LLC
K180213	01/25/2018	Titanium TomoFix Medial High Tibia Plate Anatomical	Synthes (USA) Products, LLC
K182154	08/09/2018	Depuy Synthes Femoral Neck System	Synthes (USA) Products, LLC
K180544	03/01/2018	DePuy Synthes Static Staples	Synthes (USA) Products, LLC
K150796	03/26/2015	Dental Bone Cutting Instruments	SYNTHES (USA) PRODUCTS, LLC