Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) is an AI-enabled medical device from Mighty Oak Medical, listed by FDA (510(k), K251532) with a decision date of 2025-11-03. Review panel: Radiology.
| FDA submission number | K251532 |
|---|---|
| Pathway | 510(k) |
| Company | Mighty Oak Medical |
| Review panel (specialty) | Radiology |
| FDA decision date | 2025-11-03 |
| Decision | Substantially Equivalent |
| Product code | LLZ |
| Classification | System, Image Processing, Radiological |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 168 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
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Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.