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FDA 510(k) Applications Submitted by ORTHOPRO LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K122936
09/24/2012
ANKLE TRAUMA SYSTEM
ORTHOPRO LLC
K070555
02/27/2007
ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES
ORTHOPRO LLC
K113006
10/07/2011
I-FUSE HAMMER TOE SYSTEMS
ORTHOPRO LLC
K071243
05/03/2007
METAL HEMI IMPLANT
ORTHOPRO LLC
K062908
09/27/2006
ORTHROPRO HEMI TOE
ORTHOPRO LLC
K093055
09/30/2009
CSTS SCREW
ORTHOPRO LLC
K073228
11/15/2007
DC ULNAR SHORTENING SYSTEM
ORTHOPRO LLC
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