Medical Device Manufacturer · US , Irvine , CA

Interpore Cross Intl. - FDA 510(k) Cleared Devices

39 submissions · 38 cleared · Since 1998

39

Total

38

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interpore Cross Intl. General Hospital ✕

2 devices

1-2 of 2

Cleared Apr 30, 2001

APPLICATOR TIP/DUAL SPRAYER KIT

General Hospital · 52d

Cleared Jul 31, 1998

MANIFOLD WITH EXTENSION SET

General Hospital · 24d