FDA 510(k) Applications Submitted by Amplify Surgical, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K211740 | 06/07/2021 | DualX | Amplify Surgical, Inc. |
| K222203 | 07/25/2022 | DualXSLIM(R) T/PLIF | Amplify Surgical, Inc. |
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