FDA 510(k) Application Details - K162158

Device Classification Name	Bone Grafting Material, Animal Source   More FDA Info for this Device
510(K) Number	K162158
Device Name	Bone Grafting Material, Animal Source
Applicant	Collagen Matrix, Inc. 15 Thornton Road Oakland, NJ 07436 US Other 510(k) Applications for this Company
Contact	Peggy Hansen Other 510(k) Applications for this Contact
Regulation Number	872.3930   More FDA Info for this Regulation Number
Classification Product Code	NPM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2016
Decision Date	02/09/2017
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