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Biomet Trauma

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K091976 BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAILHSB2009-08-17 View
510(k) K092078 OPTILOCK PERIARTICULAR PLATINGHRS2009-08-05 View
510(k) K082874 BIODRIVE CANNULATED SCREW SYSTEMHWC2009-02-05 View
510(k) K081244 LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONSKTT2008-07-30 View
510(k) K081243 BIOMET PHOENIX ANKLE NAIL SYSTEMHSB2008-06-27 View
510(k) K071325 BIOMET VARIABLE LOCKING PLATE SYSTEMHRS2007-07-26 View
510(k) K070823 GROWTH CONTROL PLATING SYSTEMHRS2007-05-07 View
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