Biomet Manufacturing, Inc.
Biomet Manufacturing, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2013.
Top product codes for Biomet Manufacturing, Inc.
Recent clearances by Biomet Manufacturing, Inc.
- K130390 — COMPREHENSIVE CONVERTIBLE GLENOID
- K113271 — METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS
- K113121 — COMPREHENSIVE REVERSE SHOULDER
- K080685 — HIPLOC COMPRESSION HIP SCREW
- K080088 — BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS
- K071271 — BIOMET CABLE SYSTEM
- K070399 — 100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES
- K063515 — TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE
- K061340 — 23 MM SINGLE-PEG PATELLA COMPONENT
- K061433 — VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE
- K053505 — REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS
- K052639 — GENERATION 4 POLISHED FEMORAL HIP PROSTHESIS WITH PROXIMAL CEMENT SPACER
- K052089 — XR-SERIES BI-METRIC FEMORAL COMPONENTS
- K053299 — REPICCI II ONLAY UNICOMPARTMENTAL TIBIAL COMPONENT
- K051479 — RS (REDUCED SIZE) OSS (ORTHOPEDIC SALVAGE SYSTEM) ADDITIONAL COMPONENTS
- K050028 — MAESTRO CARPAL HEMIARTHROPLASTY
- K041850 — MEDALLION MODULAR HIP SYSTEM
- K041089 — OSS BONE GRAFT SYSTEM AND OSS RAPIDSET BONE GRAFT SYSTEM
- K040610 — VERSA-DIAL HUMERAL HEAD
- K040770 — VANGUARD PATELLA COMPONENTS
- K033838 — TITANIUM TOGGLE BUTTON(S)
- K020962 — G4 SLEEVED NAIL
- K012469 — RESORBABLE NO PROFILE SCREW AND WASHER
- K012503 — METAL SCREW ANCHOR
- K010657 — COPELAND MB RESURFACING HUMERAL HEADS
- K010664 — COPELAND RESURFACING HUMERAL HEADS
- K002020 — LACTOSORB MENISCAL SCREW
- K001374 — PATIENT MATCHED COBALT ALLOY TROCHLEA REPLACEMENT
- K000262 — BOHN FEMORAL COMPONENT
- K994326 — ASCENT KNEE SYSTEM
- K993111 — ASCENT KNEE SYSTEM
- K992301 — REUNITE SCREWS
Data sourced from openFDA. This site is unofficial and independent of the FDA.