Interpore Intl. - FDA 510(k) Cleared Devices
Recent clearances: ULTRACON ULTRAFILTRATOR, PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L, INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
25
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Interpore Intl. Orthopedic ✕
1 devices