FDA 510(k) Applications Submitted by ZIMMER INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K123553	11/19/2012	ZIMMER A.T.S. 4000TS AUTOMATIC TOURNIQUET SYSTEM	ZIMMER INC.
K100111	01/14/2010	NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM	ZIMMER INC.
K123459	11/09/2012	ZIMMER PERSONA TM PERSONALIZED KNEE SYSTEM	ZIMMER INC.
K190068	01/15/2019	Vanguard XP Knee System	Zimmer Inc.
K190656	03/14/2019	Dual Mobility - Longevity and Vivacit-E Polyethylene Hip Bearings	Zimmer Inc.
K183583	12/21/2018	Vanguard Complete Knee System	Zimmer Inc.
K172114	07/13/2017	Zimmer Natural Nail System	Zimmer Inc.
K113369	11/15/2011	ZIMMER PERSONA KNEE SYSTEM	ZIMMER INC.
K191625	06/18/2019	Persona Revision Knee System	Zimmer Inc.
K181947	07/20/2018	Persona Revision Knee System	Zimmer Inc.
K122765	09/10/2012	PERSONA NATURAL TIBIA BASEPLATES	ZIMMER INC.
K191814	07/05/2019	Alliance Glenoid	Zimmer Inc.
K213856	12/10/2021	Identity Shoulder System	Zimmer Inc.
K193180	11/18/2019	Alliance Augmented Glenoid	Zimmer Inc.
K111447	05/24/2011	ZIMMER PERIARTICULAR SCREWS	ZIMMER INC.
K060556	03/02/2006	BRIGIT SURGICAL DEVICE	ZIMMER INC.