Orthopaedic & Spine Development is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Orthopaedic & Spine Development - FDA 510(k) Cleared Devices
Recent clearances: Origin™ Anterior Cervical Plate System
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.
510(k) submissions have been managed by Phiama, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Orthopaedic & Spine Development
1 devices