FDA 510(k) Applications Submitted by AlloSource
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170957 | 03/31/2017 | ReConnex Pre-Sutured Tendon | AlloSource |
| K213046 | 09/22/2021 | AceConnex Pre-Sutured Fascia | AlloSource |
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