FDA 510(k) Application Details - K250141

Device Classification Name	Filler, Bone Void, Calcium Compound   More FDA Info for this Device
510(K) Number	K250141
Device Name	Filler, Bone Void, Calcium Compound
Applicant	Austin Medical Ventures, Inc. 3012 Centre Oak Way, Suite 102 Germantown, TN 38138 US Other 510(k) Applications for this Company
Contact	Austin Brian 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	01/17/2025
Decision Date	05/16/2025
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