FDA 510(k) Application Details - K151584

Device Classification Name	Filler, Bone Void, Calcium Compound   More FDA Info for this Device
510(K) Number	K151584
Device Name	Filler, Bone Void, Calcium Compound
Applicant	PROGENTIX ORTHOBIOLOGY B.V. PROF. BRONKHORSTLAAN 10 BLDG. 48 BILTHOVEN 3723 MB NL Other 510(k) Applications for this Company
Contact	YVONNE P. BOVELL 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	06/11/2015
Decision Date	10/08/2015
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