FDA 510(k) Application Details - K250556

Device Classification Name	Filler, Bone Void, Calcium Compound   More FDA Info for this Device
510(K) Number	K250556
Device Name	Filler, Bone Void, Calcium Compound
Applicant	Ventris Medical 1201 Dove Street, Suite 470 Newport Beach, CA 92660 US Other 510(k) Applications for this Company
Contact	John Brunelle Other 510(k) Applications for this Contact
Regulation Number	888.3045   More FDA Info for this Regulation Number
Classification Product Code	MQV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/25/2025
Decision Date	03/21/2025
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