FDA 510(k) Application Details - K223913

Device Classification Name	Catheter, Thrombus Retriever   More FDA Info for this Device
510(K) Number	K223913
Device Name	Catheter, Thrombus Retriever
Applicant	Scientia Vascular Inc 3487 West 2100 South Suite 100 West Valley City, UT 84119 US Other 510(k) Applications for this Company
Contact	Thomas Lippert Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	NRY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/29/2022
Decision Date	09/20/2023
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