Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)
Mighty Oak Medical · K252103
FDA-authorized Predetermined Change Control Plan
- Company
- Mighty Oak Medical
- 510(k)/De Novo #
- K252103
- Decision date
- 2025-12-02
- Panel
- Radiology
- Pathway
- 510(k)
- Category
- AI/SaMD
- PCCP type
- Retraining
- Monitoring commitment
- Not stated
What this PCCP covers. Permits model retraining with additional data
Other PCCPs from Mighty Oak Medical
Other Radiology PCCPs
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- K254131BACDeepHealth, Inc.2026-05-21AI/SaMDI/O expansion
- K254013SubtleHD-PET (1.x)Subtle Medical, Inc.2026-05-14AI/SaMDRetraining
- K253689syngo Dynamics (VA41F)Siemens Healthcare GmbH2026-04-10AI/SaMDRetraining
- K253270Contour ProtégéAI+Mim Software, Inc.2026-03-27AI/SaMDRetraining
- K253593Clarius Ejection Fraction AIClarius Mobile Health Corp.2026-03-02AI hardwareI/O expansion
Want the monitoring teardown?
We read the PCCP for Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX), then map the post-market monitoring that its modification protocol requires, including the deployment-period evidence most teams can't reconstruct at modification time. Sentir is the independent system of record that produces it.
Book a callSource: U.S. FDA public records (openFDA 510(k)/De Novo databases and accessdata.fda.gov). PCCP type and category are editorial classifications based on public documents, not official FDA designations.
This page is a factual summary of public FDA records. Sentir Health is not affiliated with or endorsed by the named companies or the U.S. Food and Drug Administration. Spot an error? Request a correction.