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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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