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FDA 510(k) Applications Submitted by Meenakshi Gupta
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200227
01/30/2020
Journey II XR Knee Instrument
Smith & Nephew, Inc
K190730
03/21/2019
IODOSORB
Smith & Nephew Medical Ltd.
K190756
03/25/2019
IODOFLEX
Smith & Nephew Medical Ltd.
K191211
05/06/2019
JOURNEY II Unicompartmental Knee System
Smith & Nephew, Inc.
K182109
08/03/2018
REDAPT Modular Acetabular Shell
Smith & Nephew, Inc.
K182535
09/14/2018
R3 Anteverted Liners
Smith & Nephew, Inc.
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