FDA 510(k) Applications Submitted by Jenny Jiang

FDA 510(k) Number Submission Date Device Name Applicant
K190567 03/06/2019 KeYi Spinal Fixation System Beijing KeYi Medical Device Technology Co., Ltd.
K151376 05/22/2015 superDimension Navigation System Covidien LLC
K191826 07/08/2019 KeYi Total Hip System Beijing KeYi Medical Device Technology Co., Ltd.
K142839 09/30/2014 GenCut Core Biopsy System Covidien LLC


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