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FDA 510(k) Applications Submitted by Andy Choi
FDA 510(k) Number
Submission Date
Device Name
Applicant
K181397
05/29/2018
DualX
Innovasive, Inc.
K211740
06/07/2021
DualX
Amplify Surgical, Inc.
K181995
07/26/2018
Chiral Surgical Pedicle Screw System
Chiral Surgical
K192434
09/05/2019
DualX Lumbar Intervertebral Body Fusion Device
Amplify Surgical Inc
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