Medical Device Manufacturer · US , Deerfield , IL

Surgalign Spine Technologies - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022

Total

Cleared

Denied

Surgalign Spine Technologies has 3 FDA 510(k) cleared medical devices. Based in Deerfield, US.

Last cleared in 2023. Active since 2022. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Surgalign Spine Technologies

3 devices

1-3 of 3