FDA 510(k) Application Details - K053160

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K053160
Device Name	Device, Neurovascular Embolization
Applicant	MICRUS ENDOVASCULAR CORPORATION 610 PALOMAR AVENUE SUNNYVALE, CA 94085 US Other 510(k) Applications for this Company
Contact	MARGARET WEBBER 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	11/14/2005
Decision Date	12/07/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review