Medical Device Manufacturer · US , Warsaw , IN

Biomet Orthopedics, Inc. - FDA 510(k) Cleared Devices

34 submissions · 34 cleared · Since 2000

Recent clearances: E-POLY TIBIAL BEARINGS, INNERVUE DIAGNOSTIC SCOPE SYSTEM, ACID ETCHED LAG SCREWS

34

Total

34

Cleared

0

Denied

FDA 510(k) Regulatory Record - Biomet Orthopedics, Inc. Orthopedic ✕

34 devices

1-12 of 34

Cleared Jun 17, 2008

E-POLY TIBIAL BEARINGS

Orthopedic · 112d

Cleared Jan 14, 2008

INNERVUE DIAGNOSTIC SCOPE SYSTEM

Orthopedic · 97d

Cleared Oct 12, 2007

ACID ETCHED LAG SCREWS

Orthopedic · 190d

Cleared Jun 30, 2004

LACTOSCREW SCREW ANCHOR

Orthopedic · 254d

Cleared Nov 20, 2003

CALCIGEN PSI BONE GRAFT SUBSTITUTE

Orthopedic · 119d

Cleared Feb 05, 2003

HA PMI FEMORAL HIP STEM

Orthopedic · 30d

Cleared Jan 09, 2003

PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM

Orthopedic · 29d

Cleared Dec 13, 2002

COMPREHENSIVE HUMERAL FRACTURE SYSTEM

Orthopedic · 88d

Cleared Dec 11, 2002

PRESS-FIT HEAD RESURFACING DEVICE

Orthopedic · 78d

Cleared Nov 06, 2002

ARCPM 1050 RESIN-HIPS

Orthopedic · 30d

Cleared Oct 25, 2002

RINGLOC CONSTRAINED LINERS

Orthopedic · 158d

Cleared Oct 17, 2002

RX 90 FEMORAL STEM AND RX 90 LATERALIZED FEMORAL STEM

Orthopedic · 30d