FDA 510(k) Application Details - K120330

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K120330
Device Name	Device, Neurovascular Embolization
Applicant	PENUMBRA, INC. 1351 HARBOR BAY PARKWAY ALAMEDA, CA 94502 US Other 510(k) Applications for this Company
Contact	EMILLY T NURTHEN 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	02/02/2012
Decision Date	04/02/2012
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