Axis Spine Technologies, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Axis Spine Technologies, Ltd. has 2 FDA 510(k) cleared medical devices. Based in St. Albans, GB.
Last cleared in 2021. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Axis Spine Technologies, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Axis Spine Technologies, Ltd.
2 devices