Medical Device Manufacturer · US , Indianapolis , IN

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

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Life Spine, LLC has 2 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 2 cleared submissions from 2004 to 2014. Primary specialty: Orthopedic.

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

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

2 devices

1-2 of 2