Spinenet, LLC is one of 11615 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spinenet, LLC - FDA 510(k) Cleared Devices
Recent clearances: SpineNet SSP System, DAYTONA ANTERIOR CERVICAL CAGE
2
Total
2
Cleared
0
Denied
Spinenet, LLC has 2 FDA 510(k) cleared medical devices. Based in Round Rock, US.
Historical record: 2 cleared submissions from 2011 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinenet, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Spinenet, LLC
2 devices