Biomet Manufacturing, Inc.
FDA 510(k) medical device clearances.
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.