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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 K190847
Device Name REDAPT Blade Augments
Applicant
Smith & Nephew, Inc.
1450 Brooks Road
Memphis,  TN  38116
Applicant Contact Konrad Wolfmeyer
Correspondent
Smith & Nephew, Inc.
1450 Brooks Road
Memphis,  TN  38116
Correspondent Contact Konrad Wolfmeyer
Regulation Number888.3358
Classification Product Code
LPH  
Date Received04/01/2019
Decision Date 10/25/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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