Medical Device Manufacturer · US , Washington , DC

Spineguard S.A. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2013

Total

Cleared

Denied

Spineguard S.A. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2022. Active since 2013. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Spineguard S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Spineguard S.A.

6 devices

1-6 of 6