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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name prosthesis, hip, semi-constrained, metal/polymer, cemented
510(k) Number K110290
Device Name EXETER HIP STEM
Applicant
HOWMEDICA OSTEONICS CORP
325 CORPORATE DR.
mahwah,  NJ  07430
Applicant Contact valerie giambanco
Correspondent
HOWMEDICA OSTEONICS CORP
325 CORPORATE DR.
mahwah,  NJ  07430
Correspondent Contact valerie giambanco
Regulation Number888.3350
Classification Product Code
JDI  
Date Received02/01/2011
Decision Date 09/27/2011
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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