FDA 510(k) Application Details - K070055

Device Classification Name	Bone Grafting Material, Synthetic   More FDA Info for this Device
510(K) Number	K070055
Device Name	Bone Grafting Material, Synthetic
Applicant	VIVOXID LTD. 6470 RIVERVIEW TERRACE FRIDLEY, MN 55432 US Other 510(k) Applications for this Company
Contact	CONSTANCE G BUNDY 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	01/04/2007
Decision Date	06/25/2007
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