FDA 510(k) Application Details - K233562

Device Classification Name	Recorder,Event,Implantable Cardiac,(With Arrhythmia Detection)   More FDA Info for this Device
510(K) Number	K233562
Device Name	Recorder,Event,Implantable Cardiac,(With Arrhythmia Detection)
Applicant	Medtronic, Inc. 8200 Coral Sea Street NE Mounds View, MN 55112 US Other 510(k) Applications for this Company
Contact	Kerry Luyster Other 510(k) Applications for this Contact
Regulation Number	870.1025   More FDA Info for this Regulation Number
Classification Product Code	MXD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/06/2023
Decision Date	12/06/2023
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