Medical Device Manufacturer · US , Jacksonville , FL

Spine Next America Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Spine Next America Corporation has 2 FDA 510(k) cleared medical devices. Based in Jacksonville, US.

Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Spine Next America Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spine Next America Corporation

2 devices

1-2 of 2