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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bone Grafting Material, Synthetic
510(k) Number K033110
Device Name C-GRAFT
Applicant
THE CLINICIAN'S PREFERENCE LLC
388 MARKET STREET, SUITE 500
SAN FRANCISCO,  CA  94111
Applicant Contact CHARLES L MORIN
Correspondent
THE CLINICIAN'S PREFERENCE LLC
388 MARKET STREET, SUITE 500
SAN FRANCISCO,  CA  94111
Correspondent Contact CHARLES L MORIN
Regulation Number872.3930
Classification Product Code
LYC  
Date Received09/30/2003
Decision Date 12/10/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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