FDA 510(k) Application Details - K232154

Device Classification Name	More FDA Info for this Device
510(K) Number	K232154
Device Name	MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation
Applicant	MiRus, LLC 1755 West Oak Parkway, Suite 100 Marietta, GA 30062 US Other 510(k) Applications for this Company
Contact	Jordan Bauman Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/20/2023
Decision Date	09/11/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review