FDA 510(k) Applications Submitted by Arthex, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172612 | 08/31/2017 | FiberTak DX | Arthex, Inc |
| K151256 | 05/12/2015 | Arthrex BioSync« Bone Wedge | Arthex, Inc |
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