Spinevision, S.A.S. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
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.
510(k) submissions have been managed by Lince Consulting, LLC as regulatory consultant.
5 devices