FDA 510(k) Application Details - K063774

Device Classification Name	Catheter, Thrombus Retriever   More FDA Info for this Device
510(K) Number	K063774
Device Name	Catheter, Thrombus Retriever
Applicant	CONCENTRIC MEDICAL, INC. 1380 SHOREBIRD WAY MOUNTAIN VIEW, CA 94043 US Other 510(k) Applications for this Company
Contact	KIRSTEN VALLEY Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	NRY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/21/2006
Decision Date	01/24/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review