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FDA 510(k) Applications Submitted by Sejin Ryu
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170313
02/01/2017
ARIX Ankle Distal Tibia System
Jeil Medical Corporation
K170979
04/03/2017
ARIX Ankle Fibula Hook Plate System
Jeil Medical Corporation
K221412
05/16/2022
ARIX Rib System
Jeil Medical Corporation
K201656
06/18/2020
ARIX Elbow System
Jeil Medical Corporation
K172008
07/03/2017
ARIX Humerus System
Jeil Medical Corporation
K161864
07/07/2016
ARIX Foot System
JEIL MEDICAL CORPORATION
K192417
09/04/2019
ARIX Cannulated Screw System
Jeil Medical Corporation
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