Medical Device Manufacturer · US , Washington , DC

Aurora Spine, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2014

Total

Cleared

Denied

Aurora Spine, Inc. has 7 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2022. Active since 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Aurora Spine, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Aurora Spine, Inc.

7 devices

1-7 of 7