Spineguard S.A. - FDA 510(k) Cleared Devices

Spineguard S.A. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2022. Active since 2013. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Spineguard S.A. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Hogan Lovells US LLP and Hogan Lovells Llp.