Orthopaedic & Spine Development - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Orthopaedic & Spine Development has 1 FDA 510(k) cleared medical devices. Based in Avignon Cedex 9, FR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthopaedic & Spine Development Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Orthopaedic & Spine Development
1 devices