In addition to the QDOT-FAST Study, Biosense Webster is also currently enrolling and treating patients in a U.S. Investigational Device Exemption (IDE) study of QDOT MICRO.
An estimated 33 million people worldwide have been diagnosed with AF and its prevalence is projected to increase significantly as the population ages.[2] Approximately 70 percent of patients with AF are between the ages of 65 and 85.[3]
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About Johnson & Johnson Medical Devices Companies
As the world's most comprehensive medical devices business, we are building on a century of experience, leveraging science and technology, to shape the future of healthcare. With unparalleled breadth, depth and reach in surgery, orthopaedics, vision and interventional solutions we are working to profoundly change the way care is delivered. We are in this for life.
About Biosense Webster, Inc.
Biosense Webster, Inc. is a global leader in the science of diagnosing and treating heart rhythm disorders. The company partners with clinicians to develop innovative technologies that improve the quality of care for arrhythmia patients worldwide. Biosense Webster, Inc. is part of the Johnson & Johnson Family of Companies. More information can be found at www.biosensewebster.com.
*Comprising the surgery, orthopaedics, vision and interventional solutions businesses within Johnson & Johnson's Medical Devices segment
**Pulmonary Vein Isolation with Very High Power–Short Duration Temperature-Controlled Lesions: The First-in-Human QDOT-FAST Multicenter Trial
***Dr. Reddy is a consultant to Biosense Webster, Inc.
The device is approved for investigational use only. It is not approved or available for sale.
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