FDA 510(k) Application Details - K082419

Device Classification Name	Filler, Bone Void, Calcium Compound   More FDA Info for this Device
510(K) Number	K082419
Device Name	Filler, Bone Void, Calcium Compound
Applicant	INTRA-LOCK INTERNATIONAL, INC. 6560 W. ROGERS CIRCLE SUITE 24 BOCA RATON, FL 33487 US Other 510(k) Applications for this Company
Contact	JEFFREY SAKOFF 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	08/22/2008
Decision Date	05/27/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review