FDA 510(k) Applications Submitted by b-ONE ORTHO, Corp
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212912 | 09/13/2021 | OneFix Biocomposite Anchors, OneFix Biocomposite Small Anchors, OneFix All Suture Anchors, OneFix Interference Screws, OneFix Cannula System | b-ONE ORTHO, Corp |
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