FDA 510(k) Applications Submitted by Shereen Bienz

FDA 510(k) Number Submission Date Device Name Applicant
K190253 02/07/2019 EVOS Small Fragment Upper Extremity Plates Line Additions Smith & Nephew, Inc
K140555 03/04/2014 JOURNEY II BCS CONSTRAINED INSERTS SMITH & NEPHEW, INC.
K141471 06/03/2014 JOURNEY II XR KNEE SYSTEM SMITH & NEPHEW, INC.
K173331 10/23/2017 JOURNEY II XR Knee Instruments Smith & Nephew, Inc.
K143226 11/10/2014 Visionaire Disposable Instruments SMITH & NEPHEW, INC.


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