Medical Device Manufacturer · US , San Diego , CA

Kinetikos Medical, Inc. - FDA 510(k) Cleared Devices

19 submissions · 16 cleared · Since 1994
19
Total
16
Cleared
0
Denied

Kinetikos Medical, Inc. has 16 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.

Historical record: 16 cleared submissions from 1994 to 2006.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kinetikos Medical, Inc.
19 devices
1-12 of 19
Cleared Nov 22, 2006
ECLIPSE TOTAL ANKLE IMPLANT
K061749 · HSN
Orthopedic · 154d
Cleared Oct 05, 2006
KMI CEMENT RESTRICTOR IMPLANT
K061465 · JDK
Orthopedic · 132d
Cleared Sep 06, 2005
MBARESORB IMPLANT
K051611 · HWC
Orthopedic · 81d
Cleared Aug 16, 2004
KMI DISTAL VOLAR RADIUS PLATE SYSTEM
K041461 · HRS
Orthopedic · 75d
Cleared Apr 16, 2004
KATALYST RADIAL HEAD IMPLANT
K032806 · KWI
Orthopedic · 220d
Cleared Mar 01, 2004
KOMPRESSOR SCREW SYSTEM
K040356 · HWC
Orthopedic · 17d
Cleared Feb 06, 2003
KOMPRESSOR SCREW SYSTEM
K024233 · HWC
Orthopedic · 45d
Cleared Feb 05, 2003
UNIVERSAL TOTAL WRIST SYSTEM
K030037 · JWJ
Orthopedic · 30d
Cleared Dec 12, 2002
K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
K023770 · KWD
Orthopedic · 30d
Cleared May 03, 2002
MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM
K020554 · JWJ
Orthopedic · 72d
Cleared Aug 17, 1999
KMI WRIST FUSION SYSTEM
K991873 · HRS
Orthopedic · 76d
Cleared Feb 18, 1999
KMI WRIST FUSION SYSTEM
K990094 · HRS
Orthopedic · 37d
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