Spinal Kinetics / Orthofix / Seaspine - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Spinal Kinetics / Orthofix / Seaspine has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinal Kinetics / Orthofix / Seaspine Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Spinal Kinetics / Orthofix / Seaspine
1 devices