FDA 510(k) Application Details - DEN150049

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN150049
Device Name	Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm
Applicant	CONCENTRIC MEDICAL, INC. 301 EAST EVELYN AVENUE MOUNTAIN VIEW, CA 94041 US Other 510(k) Applications for this Company
Contact	JIM LEATHLEY Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	POL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/26/2015
Decision Date	09/02/2016
Decision	DENG -
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status
Type	Direct
Reviewed By Third Party	N
Expedited Review