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

FDA 510(k) cleared devices by Aurora Spine Orthopedic ✕

3 devices
1-3 of 3
Cleared Mar 24, 2025
AERO MIS Facet Fusion System
K243865 · MRW
Orthopedic · 97d
Cleared Jan 31, 2014
INTERBODY CAGE SYSTEM
K133967 · MAX
Orthopedic · 38d
Cleared Nov 27, 2013
ZIP MIS INTERSPINOUS FUSION SYSTEM
K133091 · PEK
Orthopedic · 58d
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