Spineway SA is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Spineway SA - FDA 510(k) Cleared Devices
Recent clearances: mont blanc & mont blanc MIS Spinal Systems
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.
510(k) submissions have been managed by Novus Management Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Spineway SA
2 devices