FDA 510(k) Application Details - K243593

Device Classification Name	More FDA Info for this Device
510(K) Number	K243593
Device Name	AXS Lift Intracranial Base Catheter
Applicant	Stryker Neurovascular 47900 Bayside Pkwy Fremont, CA 94538 US Other 510(k) Applications for this Company
Contact	Natalie Allen 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	11/20/2024
Decision Date	02/18/2025
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