Axis Orthopaedics - FDA 510(k) Cleared Devices
Recent clearances: Axis Chena Cervical PEEK Spacer System, AXIS 5.5 Lumbar Pedicle Screw System, Axis Anterior Cervical Plate System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Axis Orthopaedics Orthopedic ✕
3 devices