FDA 510(k) Application Details - K033110

Device Classification Name	Bone Grafting Material, Synthetic   More FDA Info for this Device
510(K) Number	K033110
Device Name	Bone Grafting Material, Synthetic
Applicant	THE CLINICIAN'S PREFERENCE LLC 388 MARKET STREET, SUITE 500 SAN FRANCISCO, CA 94111 US Other 510(k) Applications for this Company
Contact	CHARLES L MORIN Other 510(k) Applications for this Contact
Regulation Number	872.3930   More FDA Info for this Regulation Number
Classification Product Code	LYC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/30/2003
Decision Date	12/10/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review