FDA 510(k) Application Details - K931647

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K931647
Device Name	Implant, Endosseous, Root-Form
Applicant	VANCOUVER IMPLANT CENTER 3555 SYKES RD. NORTH VANCOUVER, BC CANADA V7K 2X4 CA Other 510(k) Applications for this Company
Contact	VIC MARQUES Other 510(k) Applications for this Contact
Regulation Number	872.3640   More FDA Info for this Regulation Number
Classification Product Code	DZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/05/1993
Decision Date	03/05/1996
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