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Featured Stories
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Thursday, 11 Mar 2010
The Company plans to launch the first and only premounted, balloon-expandable stent approved specifically for use in iliac arteries immediately in the USA. [more]
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Thursday, 11 Mar 2010
Engage Family offers physicians state-of-the-art introducers capable of facilitating both femoral and radial access. [more]
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Friday, 08 Jan 2010
Gore has announced the first human implants of the next generation Conformable Gore TAG thoracic endoprosthesis in the United States for the treatment of traumatic transection of the thoracic aorta. [more]
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Thursday, 04 Feb 2010
Adapt carotid nitinol stent has thinner struts to deal with tortuousity and has closed cell design to allow in-vessel conformability. [more]
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Thursday, 04 Feb 2010
Cordis Corporation, a worldwide leader in the development and manufacture of interventional vascular technology, recently announced that the Aquatrack hydrophilic nitinol guidewire, a high-performance 0.035” guidewire for physicians performing complex percutaneous interventions, has received CE marking. Cordis Corporation has an exclusive worldwide agreement with Argon Medical, the product’s manufacturer, to market and distribute Aquatrack. [more]
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Tuesday, 15 Sep 2009
This is the first of four modules covering required preclinical testing for the device. Lombard is planning to submit the next three modules with preclinical testing in the first half of 2010. [more]
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Monday, 10 Aug 2009
Approval represents a global landmark in effective peripheral intervention for treating peripheral artery disease. [more]
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Monday, 15 Jun 2009
The ClearStream Technologies’s Sleek balloon is one of the first .014” guidewire compatible rapid-exchange balloon fully dedicated to infrapopliteal vessels. [more]
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Tuesday, 05 May 2009
Pre-Investigational Device Exemption submission explores requirements for US regulator clearance for laser ablation device to treat in-stent restenosis in the legs [more]
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Monday, 27 Apr 2009
Medtronic launch THRIVE study to assess aneurysm-related mortality at five years [more]
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Wednesday, 15 Apr 2009
Medical device expands patient access to minimally-invasive treatment for aortic aneurysms [more]
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Monday, 06 Apr 2009
The latest European experience with the Anaconda stent graft was presented at the CX Symposium. [more]
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Monday, 06 Apr 2009
UK NHS National Innovation Centre identifies the VNUS Closure procedure as a “select innovative technology” [more]
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Wednesday, 01 Apr 2009
Recent FDA 510(k) clearance adds long percutaneous transluminal angioplasty balloons to Invatec’s balloon catheter line [more]
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Tuesday, 24 Mar 2009
US regulator approves 31mm version of the Gore Excluder for the treatment of abdominal aortic aneurysm [more]
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Wednesday, 18 Mar 2009
Invatec announce CE-certification for percutaneous transluminal coronary angioplasty balloon catheter, the IN.PACT Falcon [more]
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Tuesday, 10 Mar 2009
UK-based ClearStream Technologies wins FDA Approval for new line of catheters [more]
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Tuesday, 03 Mar 2009
A range of new products for the treatment of vascular disease will be launched and showcased at the CX Symposium. Aorfix (Lombard), Lifestent (Bard), Viabahn (Gore), IN.PACT (Invatec), and VenaCure EVLT (Angiodynamics) are some of the innovations available in the industry area. [more]
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Tuesday, 17 Feb 2009
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Tuesday, 17 Feb 2009
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