Medical Device Manufacturer · US , Westchester , IL

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

3 submissions · 3 cleared · Since 2006

Total

Cleared

Denied

Spinecraft, Inc. has 3 FDA 510(k) cleared medical devices. Based in Westchester, US.

Historical record: 3 cleared submissions from 2006 to 2010. Primary specialty: Orthopedic.

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

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

3 devices

1-3 of 3