FDA 510(k) Application Details - K090987

Device Classification Name	Prosthesis, Vascular Graft, Of 6mm And Greater Diameter   More FDA Info for this Device
510(K) Number	K090987
Device Name	Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
Applicant	VASCUTEK LTD. NEWMAINS AVE. INCHINNAN, RENFREWSHIRE PA4 9RR GB Other 510(k) Applications for this Company
Contact	KAREN KELSO Other 510(k) Applications for this Contact
Regulation Number	870.3450   More FDA Info for this Regulation Number
Classification Product Code	DSY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/07/2009
Decision Date	06/19/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review