Please provide your email address to receive an email when new articles are posted on . Use of an embolic protection system that employs an independent modular filter in carotid artery stenting was ...

In patients undergoing transcatheter aortic valve replacement (TAVR), a dual-filter embolic protection device enables the capture of debris traveling to the brain in 75% of cases, according to ...

WASHINGTON, DC — An embolic-protection device delivered percutaneously via the radial artery and used during transcatheter aortic-valve implantation (TAVI) in high-risk patients with aortic stenosis ...

(HealthDay News) — For patients undergoing elective carotid artery stenting (CAS), stroke/death rates are similar with use of proximal embolic protection devices (P-EPDs) and distal filter embolic ...

WASHINGTON -- An embolic protection device deployed during transcatheter aortic valve replacement (TAVR) caught plenty of material but without any impact on subclinical or clinical outcomes, the ...

DUBLIN, Oct. 9, 2020 /PRNewswire/ -- The "Embolic Protection Devices Market - Global Outlook and Forecast 2020-2025" report has been added to ResearchAndMarkets.com's offering. The market is growing ...

Renal artery stenosis is increasingly diagnosed in patients suffering from hypertension, renal insufficiency and in multivascular diseased patients. PTRA stenting is a treatment option that has a high ...

Less than a year after debuting its Wirion embolic protection system, Cardiovascular Systems is recalling all of the devices manufactured and distributed between January and November 2021. The Wirion ...

Covidien's SpiderFX is the only embolic protection device in the U.S. indicated for use in the lower extremities. (Photo: Business Wire) Embolic protection devices are used to capture and remove ...

The Wirion embolic protection system, used to capture debris or blood clots associated with atherectomy procedures in the lower extremities, has been recalled by Cardiovascular Systems Inc following ...

MUNICH — New data indicate that the debris captured by a double-filter embolic protection device varied according to valve type in patients undergoing transcatheter aortic valve replacement. “What is ...

The recall was initiated following reports of 9 device malfunctions. Cardiovascular Systems Inc. has issued a voluntary recall of unused WIRION ® Embolic Protection systems due to complaints of filter ...