![FDA, FTC and DOJ Enforcement of Medical Device Regulations FDA, FTC and DOJ Enforcement of Medical Device Regulations](https://www.fdanews.com/ext/resources/Book-Covers-2/BFFDEMDR-COVER.png?height=200&t=1685733565&width=200)
Home » MedCAD’s Patient-Specific Device Planning System Gets FDA Clearance
MedCAD’s Patient-Specific Device Planning System Gets FDA Clearance
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.
Upcoming Events
-
21Oct