FDA 510(k) Application Details - K172390

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K172390
Device Name	Device, Neurovascular Embolization
Applicant	Blockade Medical, LLC (d.b.a. Balt USA) 18 Technology Dr. Ste 169 Irvine, CA 92618 US Other 510(k) Applications for this Company
Contact	Rebecca K. Pine 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	08/08/2017
Decision Date	02/18/2018
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