Medical Device Manufacturer · US , Austin , TX

Spine360 - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Spine360 has 2 FDA 510(k) cleared medical devices. Based in Austin, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Spine360 Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spine360

2 devices

1-2 of 2