FDA 510(k) Application Details - K081432

Device Classification Name	Bone Grafting Material, Synthetic   More FDA Info for this Device
510(K) Number	K081432
Device Name	Bone Grafting Material, Synthetic
Applicant	DEPUY SPINE, INC. 325 PARAMOUNT DR. RAYNHAM, MA 02767 US Other 510(k) Applications for this Company
Contact	HANDE TUFAN 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	05/21/2008
Decision Date	08/29/2008
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