FDA 510(k) Applications Submitted by Depuy (Ireland)

FDA 510(k) Number	Submission Date	Device Name	Applicant
K192855	10/04/2019	DELTA XTEND(TM) Reverse Shoulder System	DePuy (Ireland)
K170806	03/17/2017	ATTUNE Cemented Tibial Base, Fixed Bearing	DePuy (Ireland)
K160700	03/14/2016	ATTUNE Revision Knee System	Depuy (Ireland)
K160907	04/01/2016	DePuy Actis DuoFix Hip Prosthesis	DEPUY (IRELAND)
K190344	02/14/2019	DePuy Corail AMT Hip Prosthesis	DePuy (Ireland)
K191779	07/02/2019	Attune Revision LPS Inserts	Depuy (Ireland)
K212683	08/24/2021	GLOBAL ICON Stemless Shoulder System	DePuy (Ireland)
K133834	12/17/2013	DEPUY GLOBAL UNITE SHOULDER SYSTEM	DEPUY (IRELAND)
K140881	04/07/2014	DEPUY ATTUNE KNEE SYSTEM - CEMENTLESS CR AND PS FEMORAL COMPONENETS	DEPUY (IRELAND)
K101996	07/15/2010	DEPUY GLOBAL UNITE SHOULDER SYSTEM	DEPUY (IRELAND)
K102080	07/26/2010	DEPUY RECLAIM REVISION HIP SYSTEM	DEPUY (IRELAND)
K183077	11/05/2018	Delta Xtend Reverse Shoulder System	DePuy (Ireland)