FDA 510(k) Applications Submitted by BIOMET TRAUMA

FDA 510(k) Number Submission Date Device Name Applicant
K082874 09/29/2008 BIODRIVE CANNULATED SCREW SYSTEM BIOMET TRAUMA
K091976 07/01/2009 BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAIL BIOMET TRAUMA
K081244 05/01/2008 LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS BIOMET TRAUMA
K092078 07/09/2009 OPTILOCK PERIARTICULAR PLATING BIOMET TRAUMA
K070823 03/26/2007 GROWTH CONTROL PLATING SYSTEM BIOMET TRAUMA
K081243 05/01/2008 BIOMET PHOENIX ANKLE NAIL SYSTEM BIOMET TRAUMA
K071325 05/10/2007 BIOMET VARIABLE LOCKING PLATE SYSTEM BIOMET TRAUMA


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