Medical Device Manufacturer · NL , Bilthoven

Progentix Orthobiology BV - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

Progentix Orthobiology BV has 2 FDA 510(k) cleared medical devices. Based in Bilthoven, NL.

Historical record: 2 cleared submissions from 2009 to 2015. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Progentix Orthobiology BV Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Progentix Orthobiology BV

2 devices

1-2 of 2