FDA 510(k) Application Details - K051607

Device Classification Name	Prosthesis, Hip, Cement Restrictor   More FDA Info for this Device
510(K) Number	K051607
Device Name	Prosthesis, Hip, Cement Restrictor
Applicant	NOVASPINE LLC PO BOX 969 ELMSFORD, NY 10523 US Other 510(k) Applications for this Company
Contact	HAMID KHOSROWSHAHI Other 510(k) Applications for this Contact
Regulation Number	878.3300   More FDA Info for this Regulation Number
Classification Product Code	JDK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/2005
Decision Date	10/07/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review