Medical Device Manufacturer · US , Minneapolis , MN

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

4 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Centerpulse Spine-Tech, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 2002 to 2004. Primary specialty: Orthopedic.

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

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

4 devices

1-4 of 4