Medical Device Manufacturer · US , Douglassville , PA

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

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

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

Historical record: 5 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Spinevision S.A.

5 devices

1-5 of 5