FDA 510(k) Application Details - K242516

Device Classification Name	Orthosis, Cervical Pedicle Screw Spinal Fixation   More FDA Info for this Device
510(K) Number	K242516
Device Name	Orthosis, Cervical Pedicle Screw Spinal Fixation
Applicant	MiRus, LLC 1755 W. Oak Parkway Suite 100 Marietta, GA 30062 US Other 510(k) Applications for this Company
Contact	Anuradha Nagulapati Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	NKG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/23/2024
Decision Date	11/19/2024
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