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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