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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Prosthesis, Elbow, Constrained, Cemented
510(k) Number K001989
FOIA Releasable 510(k) K001989
Device Name COONRAD/MORREY TOTAL ELBOW. MODEL 32-8105 SERIES
Applicant
Zimmer, Inc.
P.O. Box 708
Warsaw,  IN  46581 -0708
Applicant Contact LAURA D WILLIAMS
Correspondent
Zimmer, Inc.
P.O. Box 708
Warsaw,  IN  46581 -0708
Correspondent Contact LAURA D WILLIAMS
Regulation Number888.3150
Classification Product Code
JDC  
Date Received06/29/2000
Decision Date 07/25/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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