FDA greenlights Rivanna’s AI musculoskeletal imaging system

With FDA clearance in hand, Rivanna highlighted that it will accelerate the development of further AI capabilities for the Accuro XV system.

Rivanna’s Accuro XV has secured US Food and Drug Administration (FDA) clearance, setting the stage for the artificial intelligence (AI)-based musculoskeletal imaging system’s commercialisation across hospitals and medical clinics in the US.

Accuro XV uses ultrasound-based bone and 3D soft-tissue imaging technology, along with employing AI-based software to automate the detection and volumetric assessment of skeletal fractures and soft tissue injuries.

Designed for use at the point-of-triage, the system is intended to streamline emergency department workflows, hasten the evaluation of low-severity extremity injuries, and reduce reliance on x-ray referrals, Rivanna stated. 

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