Biomet Orthopedics, Inc.

FDA 510(k) & PMA Approved Devices — 35 products

Total Devices35

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K253515	Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments	JDI	2026-08-24	View
510(k)	K080528	E-POLY TIBIAL BEARINGS	JWH	2008-06-17	View
510(k)	K072879	INNERVUE DIAGNOSTIC SCOPE SYSTEM	HRX	2008-01-14	View
510(k)	K070955	ACID ETCHED LAG SCREWS	HSB	2007-10-12	View
510(k)	K033355	LACTOSCREW SCREW ANCHOR	HWC	2004-06-30	View
510(k)	K032286	CALCIGEN PSI BONE GRAFT SUBSTITUTE	MQV	2003-11-20	View
510(k)	K030048	HA PMI FEMORAL HIP STEM	LPH	2003-02-05	View
510(k)	K024086	PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM	HWC	2003-01-09	View
510(k)	K023063	COMPREHENSIVE HUMERAL FRACTURE SYSTEM	KWT	2002-12-13	View
510(k)	K023188	PRESS-FIT HEAD RESURFACING DEVICE	KXA	2002-12-11	View
510(k)	K023357	ARCPM 1050 RESIN-HIPS	LPH	2002-11-06	View
510(k)	K021661	RINGLOC CONSTRAINED LINERS	KWZ	2002-10-25	View
510(k)	K023085	RX 90 FEMORAL STEM AND RX 90 LATERALIZED FEMORAL STEM	JDI	2002-10-17	View
510(k)	K022515	BIOMET CALCANEAL PLATE	HRS	2002-09-17	View
510(k)	K022463	HA MODULAR REACH PROXIMAL POROUS AND HA MODULAR REACH COLLARED PROXIMAL POROUS FEMORAL STEMS	LPH	2002-08-16	View
510(k)	K022586	ANTERIOR STABILIZED TIBIAL BEARINGS	JWH	2002-08-15	View
510(k)	K021254	LACTOSORB MINI INTERFERENCE SCREW	HWC	2002-07-17	View
510(k)	K021799	CEMENTED FEMORAL HEAD RESURFING DEVICE	KXA	2002-06-26	View
510(k)	K013790	CALCIGEN-S BONE VOID FILER	MQV	2002-06-11	View
510(k)	K021403	HA MALLORY/HEAD POROUS FEMORAL STEM & HA MALLORY/HEAD POROUS LATERALIZED FEMORAL STEM	MEH	2002-05-31	View