Medical Device Manufacturer · US , Allendale , NJ

Osteonics Reconstructive Products Div. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1989

Total

Cleared

Denied

Osteonics Reconstructive Products Div. has 1 FDA 510(k) cleared medical devices. Based in Allendale, US.

Historical record: 1 cleared submissions from 1989 to 1990. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Osteonics Reconstructive Products Div. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Osteonics Reconstructive Products Div.

2 devices

1-2 of 2