Medical Device Manufacturer · US , New York , NY

Paradigm Spine - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2008

Total

Cleared

Denied

Paradigm Spine has 3 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2022. Active since 2008. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Paradigm Spine Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Paradigm Spine

3 devices

1-3 of 3