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

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.

Regulatory submissions have been managed by Watershed Idea Foundry, Mcra, LLC and RQM+.