Medical Device Manufacturer · US , La Jolla , CA

Fixano SA - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

Fixano SA has 5 FDA 510(k) cleared medical devices. Based in La Jolla, US.

Historical record: 5 cleared submissions from 2001 to 2002. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Fixano SA

5 devices

1-5 of 5