Medical Device Manufacturer · US , Queenstown , MD

Spine Next SA - FDA 510(k) Cleared Devices

3 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Spine Next SA has 1 FDA 510(k) cleared medical devices. Based in Queenstown, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Spine Next SA Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spine Next SA

3 devices

1-3 of 3