FDA 510(k) Application Details - K950306

Device Classification Name	Bone Grafting Material, Synthetic   More FDA Info for this Device
510(K) Number	K950306
Device Name	Bone Grafting Material, Synthetic
Applicant	IMTEC CORP. 2007 N. COMMERCE P.O. BOX 1562 ARDMORE, OK 73402 US Other 510(k) Applications for this Company
Contact	E. S GILLESPIE 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	01/25/1995
Decision Date	02/06/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review