Bonesupport AB - FDA 510(k) Cleared Devices

Bonesupport AB has 6 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Latest FDA clearance: Mar 2024. Active since 2005. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Bonesupport AB Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Bruder Consulting & Venture Group as regulatory consultant.