Medtronic(US:MDT) Prnewswire·2025-09-19 12:00Core Insights - Medtronic has received FDA approval for the Altaviva device, a minimally invasive implantable tibial neuromodulation therapy aimed at treating urge urinary incontinence, which affects approximately 16 million people in the U.S. [1][2][3] - The Altaviva device is designed to improve bladder control by sending electrical impulses to the tibial nerve, and it features a 15-year battery lifespan with automatic therapy delivery [2][3]. Company Overview - Medtronic is a global leader in healthcare technology, with a mission to alleviate pain, restore health, and extend life, employing over 95,000 people across more than 150 countries [5]. - The company has a comprehensive portfolio of neuromodulation therapies for bladder control, positioning itself as the only company with such a full offering in this area [3]. Product Details - The Altaviva device is approximately half the length of a stick of chewing gum and is implanted near the ankle without the need for sedation or imaging [2]. - The device is MRI-compatible and designed for real-life needs, allowing patients to return home with therapy activated immediately after the procedure [2][3]. Market Impact - The introduction of the Altaviva device is expected to transform the treatment landscape for urge urinary incontinence, providing new hope and improved quality of life for patients [2][3]. - Medtronic plans to host an investor call to discuss the Altaviva device and its implications for the treatment of urge urinary incontinence on October 9, 2025 [3].