FDA 510(k) Application Details - K173362

Device Classification Name	Filler, Bone Void, Calcium Compound   More FDA Info for this Device
510(K) Number	K173362
Device Name	Filler, Bone Void, Calcium Compound
Applicant	Kensey Nash Corporation dba DSM Biomedical 735 Pennsylvania Drive Exton, PA 19431 US Other 510(k) Applications for this Company
Contact	Susan Pileggi 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	10/26/2017
Decision Date	04/03/2018
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