Spineway SA - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Spineway SA has 2 FDA 510(k) cleared medical devices. Based in Ecully, FR.
Historical record: 2 cleared submissions from 2016 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spineway SA Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Spineway SA
2 devices