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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer
510(k) Number K051146
Device Name TRIATHLON KNEE SYSTEM
Original Applicant
HOWMEDICA OSTEONICS CORP
325 corporate dr.
mahwah,  NJ  07430
Original Contact karen ariemma
Regulation Number888.3560
Classification Product Code
JWH  
Date Received05/04/2005
Decision Date 07/13/2005
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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