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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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