FDA 510(k) Application Details - K082664

Device Classification Name	Catheter, Peripheral, Atherectomy   More FDA Info for this Device
510(K) Number	K082664
Device Name	Catheter, Peripheral, Atherectomy
Applicant	PATHWAY MEDICAL TECHNOLOGIES, INC. 10801 120TH AVENUE NE KIRKLAND, WA 98033 US Other 510(k) Applications for this Company
Contact	KEN PERINO Other 510(k) Applications for this Contact
Regulation Number	870.4875   More FDA Info for this Regulation Number
Classification Product Code	MCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/12/2008
Decision Date	10/06/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review