MedCAD’s Patient-Specific Device Planning System Gets FDA Clearance

November 11, 2020

MedCAD has obtained 510(k) clearance for its AccuPlan system that is used to design and produce patient-specific medical devices.

The system is comprised of a variety of technologies, tools and software that help surgeons plan for surgical procedures and allow precise 3D printing and manufacturing.

Using the platform, surgeons can receive assistance in designing patient-specific medical devices from MedCAD’s biomedical design team.

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