Rubicon Spine, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rubicon Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Rubicon Lumbar Interbody Fusion System
1
Total
1
Cleared
0
Denied
Rubicon Spine, LLC has 1 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rubicon Spine, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rubicon Spine, LLC
1 devices