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