Medical Device Manufacturer · US , Warsaw , IN

Depuy France S.A.S. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

Total

Cleared

Denied

Depuy France S.A.S. has 2 FDA 510(k) cleared medical devices. Based in Warsaw, US.

Historical record: 2 cleared submissions from 2013 to 2018. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Depuy France S.A.S. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Depuy France S.A.S.

2 devices

1-2 of 2