FDA 510(k) Application Details - K122576

Device Classification Name	Catheter, Intravascular Occluding, Temporary   More FDA Info for this Device
510(K) Number	K122576
Device Name	Catheter, Intravascular Occluding, Temporary
Applicant	STRYKER NEUROVASCULAR 47900 BAYSIDE PARKWAY FREMONT, CA 94538 US Other 510(k) Applications for this Company
Contact	JAMES LEATHLEY Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	MJN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/23/2012
Decision Date	01/11/2013
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