Medical Device Manufacturer · US , Walker , MI

Interpore Intl. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1984

25

Total

25

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interpore Intl. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jun 03, 1997

ODONTIT AUTOGENOUS BONE COLLECTION DEVICE

General & Plastic Surgery · 75d