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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