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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K870213
Device Name MODIFIED PROFILE FEMORAL HIP
Applicant
Depuy, Inc.
P.O. Box 988
Warsaw,  IN  46581
Applicant Contact STEVEN J WENTWORTH
Correspondent
Depuy, Inc.
P.O. Box 988
Warsaw,  IN  46581
Correspondent Contact STEVEN J WENTWORTH
Date Received01/20/1987
Decision Date 02/06/1987
Decision Substantially Equivalent (SESE)
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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