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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