FDA 510(k) Applications Submitted by Thomas A Slater
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K213836 | 12/09/2021 | Intracept Intraosseous Nerve Ablation System | Relievant Medsystems, Inc. |
| K222281 | 07/29/2022 | Intracept Intraosseous Nerve Ablation System | Relievant Medsystems, Inc. |
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