Spinal Edge, LLC is one of 20585 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spinal Edge, LLC - FDA 510(k) Cleared Devices
Recent clearances: ATLAS INTERVERTEBRAL BODY CAGE, SPINAL EDGE TITAN PEDICLE SCREW SYSTEM, ATLAS SPINAL CAGE, MODELS SC-150-007, 009, 011, 013, 015, 017.
3
Total
3
Cleared
0
Denied
Spinal Edge, LLC has 3 FDA 510(k) cleared medical devices. Based in Westlake, US.
Historical record: 3 cleared submissions from 2006 to 2010. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinal Edge, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spinal Edge, LLC
3 devices