FDA 510(k) Application Details - K130142

Device Classification Name	Prosthesis, Vascular Graft, Of 6mm And Greater Diameter   More FDA Info for this Device
510(K) Number	K130142
Device Name	Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
Applicant	ATRIUM MEDICAL CORPORATION 5 WENTWORTH DR HUDSON, NH 03051 US Other 510(k) Applications for this Company
Contact	MEGAN MCCAGH, RAC, CTBS 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	01/22/2013
Decision Date	03/15/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review