FDA 510(k) Application Details - K213200

Device Classification Name	Device, Vascular, For Promoting Embolization   More FDA Info for this Device
510(K) Number	K213200
Device Name	Device, Vascular, For Promoting Embolization
Applicant	Artio Medical, Inc. 127 Independence Drive Menlo Park, CA 94025 US Other 510(k) Applications for this Company
Contact	Erdie De Peralta Other 510(k) Applications for this Contact
Regulation Number	870.3300   More FDA Info for this Regulation Number
Classification Product Code	KRD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2021
Decision Date	03/21/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review