Medical Device Manufacturer · US , Minneapolis , MN

Bonesupport AB - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 2005

Total

Cleared

Denied

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.

FDA 510(k) cleared devices by Bonesupport AB

7 devices

1-7 of 7