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. Orthopedic ✕

1 devices

1-1 of 1

Cleared Sep 25, 1998

PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05,...

Orthopedic · 206d