Axis Orthopaedics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Axis Orthopaedics has 3 FDA 510(k) cleared medical devices. Based in Soldotna, US.
Historical record: 3 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Axis Orthopaedics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Coorstek Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Axis Orthopaedics
3 devices