FDA 510(k) Applications Submitted by Arthrex, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222078 | 07/14/2022 | Arthrex SoftStitch | Arthrex, Inc |
| K230976 | 04/05/2023 | Arthrex Radiopaque FiberTape Cerclage sutures | Arthrex, Inc |
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