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FDA 510(k) Applications Submitted by KIM PHAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160923
04/04/2016
REDAPT Anteverted Cemented Liner
SMITH & NEPHEW, INC.
K171073
04/11/2017
Smith & Nephew, Inc. REDAPT Augments
Smith & Nephew, Inc.
K162303
08/17/2016
REDAPT Sleeved Monolithic Revision Stems
SMITH & NEPHEW INC.
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