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Kinetikos Medical, Inc.

FDA 510(k) & PMA Approved Devices — 19 products

Total Devices19
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K061749 ECLIPSE TOTAL ANKLE IMPLANTHSN2006-11-22 View
510(k) K061465 KMI CEMENT RESTRICTOR IMPLANTJDK2006-10-05 View
510(k) K051611 MBARESORB IMPLANTHWC2005-09-06 View
510(k) K041461 KMI DISTAL VOLAR RADIUS PLATE SYSTEMHRS2004-08-16 View
510(k) K032806 KATALYST RADIAL HEAD IMPLANTKWI2004-04-16 View
510(k) K040356 KOMPRESSOR SCREW SYSTEMHWC2004-03-01 View
510(k) K024233 KOMPRESSOR SCREW SYSTEMHWC2003-02-06 View
510(k) K030037 UNIVERSAL TOTAL WRIST SYSTEMJWJ2003-02-05 View
510(k) K023770 K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)KWD2002-12-12 View
510(k) K020554 MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEMJWJ2002-05-03 View
510(k) K991873 KMI WRIST FUSION SYSTEMHRS1999-08-17 View
510(k) K990094 KMI WRIST FUSION SYSTEMHRS1999-02-18 View
510(k) K960692 SUBTALAR MBA SYSTEMHWC1996-07-23 View
510(k) K960539 DIAO HAND SURGERY SETHXB1996-07-23 View
510(k) K961051 UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)JWJ1996-06-06 View
510(k) K960533 K3 BONE SCREW SYSTEMHWC1996-03-25 View
510(k) K960537 K2 BONE SCREW SYSTEMHWC1996-03-25 View
510(k) K950704 K4 BONE SCREW SYSTEMHWC1995-06-30 View
510(k) K924724 KINETIK GREAT TOE SYSTEMLZJ1994-01-05 View
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