FDA approves another Renal denervation system to revolutionize treatment for uncontrolled hypertension

The U.S. Food & Drug Administration (FDA) has approved two renal denervation (RDN) systems and made groundbreaking advancement in the treatment of patients with uncontrolled hypertension (HTN).

These innovative systems, developed by leading medical technology companies Medtronic, Inc (Symplicity Spyral Renal Denervation System) and ReCor Inc. (Paradise Ultrasound Renal Denervation System), have the potential to transform the lives of individuals suffering with uncontrolled HTN, who may be inadequately responsive to, or are intolerant to, anti-hypertensive medications.

The FDA's approval of these RDN systems marks a significant milestone in the field of cardiovascular medicine. This invasive procedure offers a promising therapy to this targeted population. By targeting the nerves surrounding the kidneys, the systems disrupt the signals that contribute to high blood pressure, providing patients with a potentially life-changing solution.

"The approval of the renal denervation systems by the FDA is a game-changer for both interventional cardiology and the treatment of hypertension," said Dr. George Dangas, president of SCAI. "This innovative technology has the potential to revolutionize how we approach the management of high blood pressure which has grown tremendously globally, offering patients a safe and effective treatment option."