FDA 510(k) Application Details - K250602

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K250602
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	Expanding Innovations, Inc 110 Pioneer Way, Ste 1 Mountain View, CA 94041 US Other 510(k) Applications for this Company
Contact	Robert Jaramillo Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	KWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/28/2025
Decision Date	05/20/2025
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