September 9, 2011 — GE Healthcare announced it has received commitments from more than 100 customers globally for its Alcyone technology. The Alcyone is a nuclear cardiology platform designed to help facilitate workflow efficiency and dose management while maintaining image quality. It combines cadmium zinc telluride (CZT) detectors, focused pinhole collimation, stationary data acquisition and 3-D reconstruction.

September 9, 2011 — Angioslide Ltd. announced the first procedures with its new 5 x 300 mm Proteus device for treating the superficial femoral artery (SFA). The technology combines a percutaneous transluminal angioplasty (PTA) balloon and embolic capture of particles in one device. The new 5 x 300 mm size joins Angioslide's current dedicated product line solutions for the lower limbs.

September 8, 2011 – Concentric Medical announced completion of enrollment of the TREVO Study. The TREVO Study (Thrombectomy REvascularization of large Vessel Occlusions in acute ischemic stroke) is the first evaluation of Stentriever technology in a European, multicenter, prospective clinical trial. The TREVO Study was designed to assess the ability of the Trevo System to remove the blood clots that cause strokes and to restore blood flow to the brain.

Abbott announced the initiation of ABSORB BTK, an international clinical trial evaluating the safety and efficacy of the Absorb bioresorbable vascular scaffold (BVS) for the treatment of below-the-knee (BTK) critical limb ischemia. Critical limb ischemia, a severe form of peripheral artery disease (PAD), occurs when blocked vessels impair blood flow to the lower extremities, which can eventually lead to limb amputation. Absorb restores blood flow by opening a blocked vessel and providing support to the vessel until the device dissolves within approximately two years. The first patient was enrolled into the ABSORB BTK trial by Marc Bosiers, M.D., head of the Department of Vascular Surgery at St. Blasius Hospital in Dendermonde, Belgium.

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