Spineworks, LLC is one of 20314 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spineworks, LLC - FDA 510(k) Cleared Devices
Recent clearances: SPINEWORKS ANTERIOR LUMBAR DEVICE, A-WEDGE ANTERIOR INTERBODY SYSTEM (A-WEDGE A.I.S.), FIXXSURE CROSS LINK
4
Total
4
Cleared
0
Denied
Spineworks, LLC has 4 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 4 cleared submissions from 2005 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spineworks, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spineworks, LLC
4 devices