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Orthopro, LLC

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K122936 ANKLE TRAUMA SYSTEMHRS2013-02-28 View
510(k) K113006 I-FUSE HAMMER TOE SYSTEMSHWC2012-05-25 View
510(k) K093055 CSTS SCREWHWC2010-11-22 View
510(k) K073228 DC ULNAR SHORTENING SYSTEMHRS2008-02-29 View
510(k) K070555 ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRESHTY2007-07-13 View
510(k) K071243 METAL HEMI IMPLANTKWD2007-05-23 View
510(k) K062908 ORTHROPRO HEMI TOEKWD2006-11-13 View
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