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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