Paradigm Spine GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paradigm Spine GmbH - FDA 510(k) Cleared Devices
Recent clearances: Fortilink Cages with TiPlus Technology, CoFix System
2
Total
2
Cleared
0
Denied
Paradigm Spine GmbH has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Paradigm Spine GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Paradigm Spine GmbH
2 devices