FDA 510(k) Application Details - K203432

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K203432
Device Name	Device, Neurovascular Embolization
Applicant	Micro Therapeutics, Inc. d/b/a ev3 Neurovascular 5290 California Ave Irvine, CA 92617 US Other 510(k) Applications for this Company
Contact	Bhavika Patel 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	11/23/2020
Decision Date	07/07/2021
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