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Johnson & Johnson Company

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K063577 FEMORAL INTRAFIX SCREW AND SHEATHMBI2007-01-25 View
510(k) K060914 TRIDENT ANCHORHWC2006-06-09 View
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