Medical Device Manufacturer · US , Washington , DC

Aurora Spine - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2013
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.

FDA 510(k) cleared devices by Aurora Spine

3 devices
1-3 of 3
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All3 Orthopedic 3