Biomet Trauma
Biomet Trauma holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2009.
Top product codes for Biomet Trauma
Recent clearances by Biomet Trauma
- K091976 — BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAIL
- K092078 — OPTILOCK PERIARTICULAR PLATING
- K082874 — BIODRIVE CANNULATED SCREW SYSTEM
- K081244 — LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS
- K081243 — BIOMET PHOENIX ANKLE NAIL SYSTEM
- K071325 — BIOMET VARIABLE LOCKING PLATE SYSTEM
- K070823 — GROWTH CONTROL PLATING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.