PrecisionOS Gets FDA’s 510(k) Clearance for Its VR Surgical Planning Tool

PrecisionOS has received the FDA’s 510(k) clearance for its InVisionOS a patient-specific planning tool using virtual reality (VR).

The software automatically converts the patient's computed tomography scan from any picture archiving system into a 3D reconstruction within seconds. Surgeons can then use the Oculus Quest 2 to view and isolate relevant anatomical areas before surgery.

The patented software will be available on the U.S. market in early 2022, according to the Vancouver, Canada-based company.