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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name plate, fixation, bone
510(K) Number K782123
Device Name MULTIPLICITY OF PRODUCTS
Applicant
DEPUY, INC.
Regulation Number888.3030
Classification Product Code
HRS  
Date Received12/27/1978
Decision Date 01/10/1979
Decision substantially equivalent (SE)
Classification Advisory Committee Orthopedic
Review Advisory Committee Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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