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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 K810326
Device Name POROCOAT TM TOWNLEY ANATOMIC KNEE
Applicant
DEPUY, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
DEPUY, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number888.3560
Classification Product Code
JWH  
Date Received02/09/1981
Decision Date 03/11/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
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