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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Rod, Fixation, Intramedullary And Accessories
510(k) Number K142281
Device Name ZIMMER M/DN INTRAMEDULLARY FIXATION SYSTEM
Applicant
ZIMMER, INC.
P.O. BOX 708
WARSAW,  IN  46581 -0708
Applicant Contact PATRICK MCCULLAGH
Correspondent
ZIMMER, INC.
P.O. BOX 708
WARSAW,  IN  46581 -0708
Correspondent Contact STEPHEN H. MCKELVEY
Regulation Number888.3020
Classification Product Code
HSB  
Date Received08/15/2014
Decision Date 10/22/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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