Kinetikos Medical, Inc.
Kinetikos Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2006.
Top product codes for Kinetikos Medical, Inc.
Recent clearances by Kinetikos Medical, Inc.
- K061749 — ECLIPSE TOTAL ANKLE IMPLANT
- K061465 — KMI CEMENT RESTRICTOR IMPLANT
- K051611 — MBARESORB IMPLANT
- K041461 — KMI DISTAL VOLAR RADIUS PLATE SYSTEM
- K032806 — KATALYST RADIAL HEAD IMPLANT
- K040356 — KOMPRESSOR SCREW SYSTEM
- K024233 — KOMPRESSOR SCREW SYSTEM
- K030037 — UNIVERSAL TOTAL WRIST SYSTEM
- K023770 — K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
- K020554 — MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM
- K991873 — KMI WRIST FUSION SYSTEM
- K990094 — KMI WRIST FUSION SYSTEM
- K960539 — DIAO HAND SURGERY SET
- K960692 — SUBTALAR MBA SYSTEM
- K961051 — UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)
- K960533 — K3 BONE SCREW SYSTEM
- K960537 — K2 BONE SCREW SYSTEM
- K950704 — K4 BONE SCREW SYSTEM
- K924724 — KINETIK GREAT TOE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.