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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, Porous Uncemented
510(k) Number K043537
Device Name TAPERLOC 12/14 TAPER FEMORAL COMPONENTS
Applicant
Biomet, Inc.
56 E. Bell Dr.
P.O. Box 587
Warsaw,  IN  46582
Applicant Contact PATRICIA SANDBORN BERES
Correspondent
Biomet, Inc.
56 E. Bell Dr.
P.O. Box 587
Warsaw,  IN  46582
Correspondent Contact PATRICIA SANDBORN BERES
Regulation Number888.3358
Classification Product Code
LPH  
Date Received12/22/2004
Decision Date 01/14/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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