Medical Device Manufacturer · US , Santa Clara , CA

Kinetix Instruments - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Kinetix Instruments has 1 FDA 510(k) cleared medical devices. Based in Santa Clara, US.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Kinetix Instruments Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kinetix Instruments

1 devices

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