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Home » Varian wins FDA clearance for IntelliBlate microwave ablation system

Varian wins FDA clearance for IntelliBlate microwave ablation system

July 30, 2024 By Sean Whooley

Varian IntelliBlate microwave ablation system
The IntelliBlate system. [Image from the Varian website]
Siemens Healthineers‘ Varian announced that it received FDA 510(k) clearance for its IntelliBlate microwave ablation system.

Varian designed IntelliBlate to provide greater predictability, precision and control during the ablation of soft tissue. The system produces large, controlled, spherical ablation zones for predictable treatment delivery. Users can deliver ablation with a single probe or dual probes, each linked with independent controls. The system’s Ximitry probe enables new features like laser disk alignment and intuitive LED indicators, too.

According to a news release, Varian’s ablation system design and intuitive interface deliver a portable, flexible system. Modular elements enable clinicians to expand their treatment capabilities to meet changing clinical demands, too. Despite changes and flexibility, users can still control operational efficiency throughout the ablation procedure.

Varian aims to connect more intelligent therapeutic technologies and image-guided innovations in a single platform. With IntelliBlate, clinicians get even greater predictability of probe placement, treatment delivery and procedural confirmation.

“IntelliBlate combines the features our customers say are most important for an efficient, integrated solution to seek improved levels of performance in microwave ablation,” says Dr. David Hahn, VP and chief medical officer, Varian Interventional Solutions. “This innovative system brings new versatility in treatment options, fueling clinician-driven innovation to tackle a wide variety of cases. Real-time monitoring and treatment information at the tissue level aim to further empower care teams with the confidence to deliver highly personalized care to patients.”

Filed Under: 510(k), Food & Drug Administration (FDA), Imaging, Radiosurgery/Radiation therapy, Regulatory/Compliance Tagged With: FDA, Varian, Varian Medical Systems

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About Sean Whooley

Sean Whooley is an associate editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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