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FDA 510(k) Applications Submitted by Smith & Nephew Inc
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190085
01/17/2019
Journey II Unicompartmental Knee System
Smith & Nephew Inc
K222971
09/27/2022
ULTRABUTTON QUAD Adjustable Fixation Device; ULTRABUTTON BB Adjustable Fixation Device; ULTRABUTTON TIB SMALL Adjustable Fixation Device; ULTRABUTTON TIB MEDIUM Adjustable Fixation Device; ULTRABUTTON TIB LARGE Adjustable Fixation Device
Smith & Nephew Inc
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