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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 uncemented acetabular component)
510(K) Number K850055
Device Name PROFILE FEMORAL HIP
Applicant
DEPUY, INC.
p.o. box 988
warsaw,  IN  46581 0988
Contact stephen m doyle
Regulation Number888.3330
Classification Product Code
KWA  
Date Received01/08/1985
Decision Date 04/23/1985
Decision substantially equivalent (SE)
Classification Advisory Committee Orthopedic
Review Advisory Committee Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
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