The Pipeline Vantage embolization device. [Image courtesy of Medtronic] The FDA deemed a recall of some Medtronic (NYSE: MDT) + Pipeline Vantage embolization devices serious after multiple deaths ...
March 18, 2025—The FDA announced that Medtronic initiated a device recall and correction for embolization devices. The FDA has identified this recall as the “most serious type.” According to the FDA, ...
Background Effective sealing of the aneurysm neck with a Woven Endobridge (WEB) device is crucial for disrupting the blood flow inside the aneurysm sac and promoting neck endothelialization. Using a ...
Background Sealing of the aneurysm neck with a Woven EndoBridge (WEB) device is recommended for disrupting the blood flow inside the aneurysm. This study investigates the relationship between WEB neck ...
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The U.S. FDA has cleared Aroa Biosurgery Ltd.’s 510(k) for its Enivo pump and catheter, which are key components of the company’s new Enivo tissue apposition platform. The device applies negative ...
The U.S. FDA has cleared Aroa Biosurgery Ltd.’s 510(k) for its Enivo pump and catheter, which are key components of the company’s new Enivo tissue apposition platform. The device applies negative ...
1 Department of Neurointervention Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China 2 Department of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital ...
Ask the publishers to restore access to 500,000+ books. A line drawing of the Internet Archive headquarters building façade. An illustration of a heart shape "Donate to the archive" An illustration of ...
The new RhinAer provides physicians with improved visualization, easier access and tissue apposition, according to the company. [Image from Aerin Medical] Aerin Medical announced today that it ...
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