FDA 510(k) Applications Submitted by Lai Saeteurn
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221128 | 04/18/2022 | Arthrex ACL TightRope«, PCL TightRope«, and TightRope« II | Arthrex Inc. |
| K221354 | 05/10/2022 | Arthrex SutureTape | Arthrex Inc. |
| K221396 | 05/13/2022 | Arthrex FiberTak Suture Anchor | Arthrex Inc. |
| K212146 | 07/09/2021 | Arthrex LoopLoc Knotless Suture | Arthrex, Inc. |
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