Kinetikos Medical, Inc.
FDA 510(k) medical device clearances.
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.