Medical Device Manufacturer · US , Logan , UT

Intrafuse, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017

Total

Cleared

Denied

Intrafuse, LLC has 2 FDA 510(k) cleared medical devices. Based in Logan, US.

Historical record: 2 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Intrafuse, LLC

2 devices

1-2 of 2