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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