Boston Scientific has obtained CE mark approval for its Synergy Everolimus-Eluting platinum chromium coronary stent system, designed to improve post-implant vessel healing. The coronary stent, which features a combination of ...
Global healthcare firm Abbott's everolimus eluting coronary stent system has been accorded with CE Mark in Europe. The XIENCE Xpedition everolimus eluting coronary stent system, which is used to treat coronary artery disease, provides ...
Tags: Abbott, CE mark, coronary stent system, coronary artery disease
Abbott has obtained the US Food and Drug Administration (FDA) approval for its Omnilink Elite Vascular Balloon-Expandable Stent system, designed as a treatment for atherosclerotic iliac artery lesions with reference vessel diameters of ≥ ...
Tags: Abbott, FDA, approval, Omnilink Elite stent, study, Omnilink Elite
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Flexible Stenting Solutions' additional sizes of FlexStent Biliary Self-Expanding Stent system including 9 and 10mm diameters in lengths up to 100mm. The FlexStent ...
Cardionovum is planning to launch its new Sirolimus-eluting coronary stent system, Prolimus Biograde, in Q4 2012. The new Prolimus Biograde features thin-stent strut design of just 71 microns which is designed to provide uniform stent ...
Tags: Cardionovum, Sirolimus-eluting coronary stent system, clinical product
Elixir Medical has gained CE Mark approval for its DESyne BD Novolimus Eluting Coronary Stent System with biodegradable polymer coating. The Elixir DESyne BD stent leverages the technology that enables an ultrathin (< 3 microns) polymer ...
Tags: Elixir Medical, Elixir DESyne BD stent, biodegradable polymer coating
Boston Scientific has received the US Food and Drug Administration (FDA) approval for 32 mm and 38 mm lengths of the Promus Element Plus Everolimus-Eluting Platinum Chromium Coronary Stent system. The Promus Element Stent is made with a ...
Tags: FDA, Boston Scientific, Promus Element Stent, coronary artery disease
Flexible Stenting Solutions has received CE mark approval for its FlexSten Iliac Self Expanding Stent system for the treatment of symptomatic atherosclerotic disease of the common and/or external iliac arteries. The FlexStent Iliac Stent ...
Tags: Flexible Stenting Solutions, FlexSten Iliac Self Expanding Stent system
The US Food and Drug Administration (FDA) has approved labeling changes for the Stryker Wingspan Stent System, including the indications for use. The changes were outlined by FDA in a safety communication and specify a more limited group ...
Boston Scientific has completed enrolling first patient in a EVOLVE II clinical trial of its Synergy Everolimus-Eluting platinum chromium coronary stent system. The CE-marked stent features a combination of everolimus drug and ...
Tags: Synergy Everolimus Eluting platinum chromium coronary stent system
Tryton Medical has completed enrolling patients in the pivotal study of its Tryton Side Branch Stent system, designed for treating bifurcation lesions. The CE-marked cobalt chromium stent uses a standard single-wire balloon-expandable ...
Tags: Tryton Medical, Tryton Side Branch Stent system, bifurcation lesions
Terumo Interventional Systems has completed enrolling patients in its Occlusive/Stenotic Peripheral Artery REvascularization StudY (OSPREY). The MISAGO stent comprises a nitinol stent pre-mounted on the distal portion of a rapid-exchange ...
Tags: OSPREY Trial, Misago Stent system, superficial femoral artery