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Home » FDA grants Sonivie IDE approval for resistant hypertension study
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FDA grants Sonivie IDE approval for resistant hypertension study

June 20, 2022
By Catherine Longworth
The U.S. FDA has granted Sonivie Ltd. IDE approval for a pilot study to treat resistant hypertension patients with renal artery denervation (RDN) using its Tivus ultrasound ablation system. The intravascular, catheter-based system uses high-frequency non-focused ultra-sound energy to ablate nerves in the renal artery and cause denervation of nerves in other structures such as the bronchus.
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