www.fdanews.com/articles/199974-medcads-patient-specific-device-planning-system-gets-fda-clearance
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.