Paradigm Spine, LLC - FDA 510(k) Cleared Devices

Paradigm Spine, LLC has 4 FDA 510(k) cleared orthopedic devices. Based in Washington, US.

Historical record: 4 cleared submissions from 2008 to 2016.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Musculoskeletal Clinical Regulatory Advisers, LLC as regulatory consultant.