FDA 510(k) Application Details - K202752

Device Classification Name	More FDA Info for this Device
510(K) Number	K202752
Device Name	AXS Vecta 46 Intermediate Catheter
Applicant	Stryker Neurovascular 47900 Bayside Parkway Fremont, CA 94538 US Other 510(k) Applications for this Company
Contact	Shivani H. Patel Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QJP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/21/2020
Decision Date	08/27/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review