FRIOS ALGIPORE


Device Classification Name

bone grafting material, synthetic

510(k) Number K023799
Device Name FRIOS ALGIPORE
Original Applicant
FRIADENT GMBH
21911 erie ln.
lake forest, 
CA 
92630

Original Contact carol patterson
Regulation Number 872.3930
Classification Product Code
LYC  
Date Received 11/14/2002
Decision Date 02/05/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Dental

510k Review Panel

Dental

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No