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Osteotomy Guide Co.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K861576 SHORTENING OSTEOTOMY GUIDEHTH1986-05-12 View
510(k) K860323 REESE ARTHRODESIS SCREWHWC1986-02-19 View
510(k) K841470 REESE OSTEOTOMY GUIDE SYSHTH1984-05-23 View
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