FDA 510(k) Application Details - K080379

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K080379
Device Name	Device, Neurovascular Embolization
Applicant	MICRUS ENDOVASCULAR CORPORATION 821 FOX LANE SAN JOSE, CA 95131 US Other 510(k) Applications for this Company
Contact	PATRICK LEE Other 510(k) Applications for this Contact
Regulation Number	882.5950   More FDA Info for this Regulation Number
Classification Product Code	HCG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/13/2008
Decision Date	06/30/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review