Medical Device Manufacturer · FR , Antony

Spinevision, S.A.S. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2018

Total

Cleared

Denied

Spinevision, S.A.S. has 5 FDA 510(k) cleared medical devices. Based in Antony, FR.

Last cleared in 2022. Active since 2018. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Spinevision, S.A.S.

5 devices

1-5 of 5