Medical Device Manufacturer · US , Minneapolis , MN

Corespine Technologies, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

Total

Cleared

Denied

Corespine Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Corespine Technologies, LLC

1 devices

1-1 of 1