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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 K882671
Device Name SAMUELSON SCREWLOC CUP
Applicant
PROTEK, INC.
5780 west 71st st.
indianapolis,  IN  46278
Contact kenneth epling
Regulation Number888.3330
Classification Product Code
KWA  
Date Received06/28/1988
Decision Date 10/20/1988
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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