FDA 510(k) Application Details - K211338

Device Classification Name	Catheter, Thrombus Retriever   More FDA Info for this Device
510(K) Number	K211338
Device Name	Catheter, Thrombus Retriever
Applicant	Neuravi Ltd. Block 3, Ballybrit Business Park Galway H91 K5YD IE Other 510(k) Applications for this Company
Contact	Niall Fox 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	05/03/2021
Decision Date	07/30/2021
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