Medical Device Manufacturer · US , Parsippany , NJ

Biomet Trauma - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2007
7
Total
7
Cleared
0
Denied

Biomet Trauma has 7 FDA 510(k) cleared medical devices. Based in Parsippany, US.

Historical record: 7 cleared submissions from 2007 to 2009. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Biomet Trauma Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biomet Trauma
7 devices
1-7 of 7
Cleared Aug 17, 2009
BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAIL
K091976 · HSB
Orthopedic · 47d
Cleared Aug 05, 2009
OPTILOCK PERIARTICULAR PLATING
K092078 · HRS
Orthopedic · 27d
Cleared Feb 05, 2009
BIODRIVE CANNULATED SCREW SYSTEM
K082874 · HWC
Orthopedic · 129d
Cleared Jul 30, 2008
LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS
K081244 · KTT
Orthopedic · 90d
Cleared Jun 27, 2008
BIOMET PHOENIX ANKLE NAIL SYSTEM
K081243 · HSB
Orthopedic · 57d
Cleared Jul 26, 2007
BIOMET VARIABLE LOCKING PLATE SYSTEM
K071325 · HRS
Orthopedic · 77d
Cleared May 07, 2007
GROWTH CONTROL PLATING SYSTEM
K070823 · HRS
Orthopedic · 42d
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