FDA 510(k) Applications Submitted by SpineVision SAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K193000 | 10/28/2019 | Hexanium« ACIF | SpineVision SAS |
| K210359 | 02/08/2021 | Hexanium TLIF | SpineVision SAS |
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