Biomet Orthopedics, Inc.
FDA 510(k) medical device clearances.
Top product codes for Biomet Orthopedics, Inc.
Recent clearances by Biomet Orthopedics, Inc.
- K080528 — E-POLY TIBIAL BEARINGS
- K072879 — INNERVUE DIAGNOSTIC SCOPE SYSTEM
- K070955 — ACID ETCHED LAG SCREWS
- K033355 — LACTOSCREW SCREW ANCHOR
- K032286 — CALCIGEN PSI BONE GRAFT SUBSTITUTE
- K030048 — HA PMI FEMORAL HIP STEM
- K024086 — PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM
- K023063 — COMPREHENSIVE HUMERAL FRACTURE SYSTEM
- K023188 — PRESS-FIT HEAD RESURFACING DEVICE
- K023357 — ARCPM 1050 RESIN-HIPS
- K021661 — RINGLOC CONSTRAINED LINERS
- K023085 — RX 90 FEMORAL STEM AND RX 90 LATERALIZED FEMORAL STEM
- K022515 — BIOMET CALCANEAL PLATE
- K022463 — HA MODULAR REACH PROXIMAL POROUS AND HA MODULAR REACH COLLARED PROXIMAL POROUS FEMORAL STEMS
- K022586 — ANTERIOR STABILIZED TIBIAL BEARINGS
- K021254 — LACTOSORB MINI INTERFERENCE SCREW
- K021799 — CEMENTED FEMORAL HEAD RESURFING DEVICE
- K013790 — CALCIGEN-S BONE VOID FILER
- K021403 — HA MALLORY/HEAD POROUS FEMORAL STEM & HA MALLORY/HEAD POROUS LATERALIZED FEMORAL STEM
- K020381 — EXPANDABLE KNEE
- K020963 — TAPERLOC POROUS FEMORAL STEM & HA TAPERLOC POROUS LATERALIZED FEMORAL STEM
- K020905 — NBX - NON-BRIDGING EXTERNAL FIXATOR
- K020221 — IQL BASIC FRAGMENT PLATE SET, IQL BASIC FRAGMENT SCREW SET, IQL SMALL FRAGMENT SET, IQL MINI FRAGMENT SET
- K013923 — TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER
- K020264 — REPICCI II UNICONDYLAR KNEE SYSTEM
- K020045 — 3-PIECE PROXIMAL HUMERAL REPLACEMENT SYSTEM
- K020076 — PATRIOT PROTRUSIO CAGE
- K013534 — SELF-COUNTERSINKING BONE SCREW
- K013657 — MODIFICATION TO: BIOMET HUMERAL CABLE PLATES
- K013042 — DISCOVERY ELBOW
- K010827 — COPELAND MB/HA RESURFACING HUMERAL HEADS
- K002278 — BROOKER FEMORAL NAILS
- K002057 — BROOKER TIBIA NAILS
- K001660 — MALLORY HEAD MODULAR CALCAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.