Medical Device Manufacturer · US , San Diego , CA

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

19 submissions · 16 cleared · Since 1994

Total

Cleared

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

1-19 of 19

Cleared Nov 22, 2006

ECLIPSE TOTAL ANKLE IMPLANT

K061749 · HSN

Orthopedic · 154d

Cleared Oct 05, 2006

KMI CEMENT RESTRICTOR IMPLANT

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

Cleared Jul 23, 1996

DIAO HAND SURGERY SET

UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)

KINETIK GREAT TOE SYSTEM

K924724 · LZJ

Orthopedic · 471d

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

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