FDA 510(k) Applications Submitted by Jessica Kim
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240815 | 03/25/2024 | Arthrex Cannulated Screw System | Arthrex Inc. |
| K232897 | 09/18/2023 | Arthrex Small External Fixation System | Arthrex Inc |
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