FDA 510(k) Application Details - K062553

Device Classification Name	Bone Cement   More FDA Info for this Device
510(K) Number	K062553
Device Name	Bone Cement
Applicant	STRYKER ORTHOPAEDICS 325 Corporate Drive Mahwah, NJ 07430 US Other 510(k) Applications for this Company
Contact	TIFFANI D ROGERS Other 510(k) Applications for this Contact
Regulation Number	888.3027   More FDA Info for this Regulation Number
Classification Product Code	LOD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/2006
Decision Date	01/08/2007
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