Medical Device Manufacturer · US , Irvine , CA

Biomet Interpore Cross - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Biomet Interpore Cross Dental ✕

1 devices

1-1 of 1

Cleared Jan 20, 2012

REGENEROSS ALLOGRAFT PLUS MINERLIZED