FDA 510(k) Applications Submitted by SpineVision, S.A.S.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221578 | 06/01/2022 | Hexanium ACIF | SpineVision, S.A.S. |
| K223251 | 10/21/2022 | Hexanium PLIF | SpineVision, S.A.S. |
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