Progentix Orthobiology BV is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Progentix Orthobiology BV - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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