X-Bolt Orthopaedics is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
X-Bolt Orthopaedics - FDA 510(k) Cleared Devices
Recent clearances: X-BOLT Hip Fracture Fixation System
1
Total
1
Cleared
0
Denied
X-Bolt Orthopaedics has 1 FDA 510(k) cleared medical devices. Based in Dublin, IE.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by X-Bolt Orthopaedics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Musculoskeletal Clinical Regulatory Advisers, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - X-Bolt Orthopaedics
1 devices