FDA 510(k) Application Details - K963431

Device Classification Name	Restraint, Protective   More FDA Info for this Device
510(K) Number	K963431
Device Name	Restraint, Protective
Applicant	ZIMMER, INC. 200 W. OHIO AVE. P.O. BOX 10 DOVER, OH 44622 US Other 510(k) Applications for this Company
Contact	PAULA OSORIO Other 510(k) Applications for this Contact
Regulation Number	880.6760   More FDA Info for this Regulation Number
Classification Product Code	FMQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/1996
Decision Date	11/06/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review