Medical Device Manufacturer · US , Los Altos Hills , CA

Innospine, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Total

Cleared

Denied

Innospine, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Altos Hills, US.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Innospine, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Innospine, Inc.

1 devices

1-1 of 1