This article deconstructs the IIH guidelines, contrasting medical management (acetazolamide, topiramate) with the practical ...
A 79-year-old man was admitted to a hospital in Guangzhou, China, with progressive dyspnea and edema. Echocardiography and ...
The investigational device evaluated in the trial, previously known as the GORE ® VIAFORT Vascular Stent, will now be referred to as the GORE ® VIABAHN ® FORTEGRA Venous Stent. CAUTION: ...
The MarketWatch News Department was not involved in the creation of this content. The investigational device evaluated in the trial, previously known as the GORE(R) VIAFORT Vascular Stent, will now be ...
In a pair of randomized, observer-blinded clinical trials designed to evaluate optimal management of asymptomatic carotid ...
Recana Thrombectomy Catheter System is designed to address the challenges of venous in-stent restenosis and residual thrombotic obstructions and occlusions. REDWOOD CITY, Calif., October 31, ...
Dural sinus malformation occasionally results in the development of giant venous lakes involving torcular herophili. Such dilatation can result in the formation of a ...
Medical Device Network on MSN
Gore’s venous stent study meets primary endpoint
The trial assessed the performance of the device over 12 months in individuals experiencing symptomatic deep venous disease.
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FDA clears InterVene’s in-stent restenosis catheter
InterVene’s Recana, a mechanical thrombectomy catheter designed to address venous in-stent restenosis (ISR) and clear vessel obstructions, has received 510(k) clearance from the US Food and Drug ...
InterVene, Inc., a privately held medical device company pioneering interventional devices for venous occlusions, today announced it received 510(k) clearance from the U.S. Food and Drug ...
TCT 1366: Devil's Dager or Cupid's Arrow: Percutaneous Removal of Fractured IVC Filter Strut From Across the Septum Receive the the latest news, research, and presentations from major meetings right ...
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