Vuze Medical Gets FDA’s 510(k) Clearance for Its Spine Surgery Software

Vuze Medical has received the FDA’s 510(k) clearance for its Vuze system for use in spinal surgeries.

The system is designed for use during common spinal stabilization surgeries in outpatient or ambulatory settings that are currently aided solely by X-rays.

The system overlays a graphical representation generated from the patient’s standard pre-operative scan for use in guidance and verification during minimally invasive surgery, the Israel-based company said.