Medical Device Manufacturer · US , Minneapolis , MN

Spine-Tech, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Spine-Tech, Inc. has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 3 cleared submissions from 1994 to 1998. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Spine-Tech, Inc.

4 devices

1-4 of 4