Paradigm Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paradigm Spine - FDA 510(k) Cleared Devices
Recent clearances: Fortilink with TiPlus Technology
3
Total
3
Cleared
0
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.
510(k) submissions have been managed by Surgalign Spine Technologies as regulatory consultant.
FDA 510(k) Regulatory Record - Paradigm Spine
3 devices