FDA 510(k) Application Details - K241259

Device Classification Name	Device, Percutaneous Retrieval   More FDA Info for this Device
510(K) Number	K241259
Device Name	Device, Percutaneous Retrieval
Applicant	Medtronic, Inc. 710 Medtronic Pkwy NE Minneapolis, MN 55432 US Other 510(k) Applications for this Company
Contact	Erin Roquemore Other 510(k) Applications for this Contact
Regulation Number	870.5150   More FDA Info for this Regulation Number
Classification Product Code	MMX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/06/2024
Decision Date	06/03/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review