FDA 510(k) Application Details - K961101

Device Classification Name	System, Cement Removal Extraction   More FDA Info for this Device
510(K) Number	K961101
Device Name	System, Cement Removal Extraction
Applicant	STRYKER CORP. 2725 FAIRFIELD RD. KALAMAZOO, MI 49002 US Other 510(k) Applications for this Company
Regulation Number	888.4580   More FDA Info for this Regulation Number
Classification Product Code	LZV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/1996
Decision Date	07/15/1996
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