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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
510(k) Number K131413
Device Name XTRAFIX SMALL EXTERNAL FIXATION SYSTEM
Applicant
Zimmer, Inc.
P.O. Box 708
Warsaw,  IN  46581
Correspondent
Zimmer, Inc.
P.O. Box 708
Warsaw,  IN  46581
Regulation Number888.3030
Classification Product Code
KTT  
Subsequent Product Code
JDW  
Date Received05/16/2013
Decision Date 01/28/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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