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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, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
510(k) Number K141056
Device Name TRIATHLON KNEE SYSTEM POSTERIOR STABILIZED COMPONENTS
Applicant
STRYKER ORTHOPAEDICS
325 Corporate Drive
mahwah,  NJ  07430
Applicant Contact karen ariemma
Correspondent
STRYKER ORTHOPAEDICS
325 Corporate Drive
mahwah,  NJ  07430
Correspondent Contact karen ariemma
Regulation Number888.3565
Classification Product Code
MBH  
Subsequent Product Code
JWH  
Date Received04/24/2014
Decision Date 08/05/2014
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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