Aurora Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aurora Spine - FDA 510(k) Cleared Devices
Recent clearances: AERO MIS Facet Fusion System
3
Total
3
Cleared
0
Denied
Aurora Spine has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Latest FDA clearance: Mar 2025. Active since 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Aurora Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Development as regulatory consultant.
FDA 510(k) Regulatory Record - Aurora Spine
3 devices