Medical Device Manufacturer · US , Riverside , CA

Acme Spine, LLC - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Acme Spine, LLC has 1 FDA 510(k) cleared medical devices. Based in Riverside, US.

Historical record: 1 cleared submissions from 2000 to 2007. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Acme Spine, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Acme Spine, LLC

2 devices

1-2 of 2