The Cordis Aquatrack Hydrophilic Guide Wire is designed to facilitate access to the most tortuous anatomy.

The Ostial Pro Stent Positioning System is designed to facilitate precise stent implantation in coronary and renal aorto-ostial lesions, eliminating the guesswork when deploying a stent at the “true” ostium of the vessel.

Morris Innovative offers the FISH (Femoral Introducer Sheath and Hemostasis) Device that combines one sheath as both an introducer and closure device.

October 17, 2008 - Elixir Medical Corp. today announced results from three multicenter first-in-man studies of Novolimus and Myolimus eluting coronary stent systems at the 20th Annual Transcatheter Cardiovascular Therapeutics (TCT) scientific symposium in Washington, D.C.

October 17, 2008 - Boston Scientific Corp. announced results at TCT from an analysis of the HORIZONS-AMI trial showing a 41 percent reduction in revascularization in patients with TAXUS Express Paclitaxel-eluting coronary stents as opposed to those with non-drug-eluting Express stents.

October 17, 2008 - The Medicines Company’s Angiomax (bivalirudin) significantly reduced cardiac-related death, improved overall survival and reduced major bleeding compared to conventional therapy (heparin plus a platelet glycoprotein IIb/IIIa inhibitor) in patients undergoing angioplasty for up to one year, according to data released at TCT this week from the HORIZONS-AMI study.

October 17, 2008 - Berlin Heart Inc. said yesterday that its EXCOR Pediatric ventricular assist device (VAD) has received unconditional approval from the FDA for IDE (investigation device exemption) study.
In 2007, the FDA had granted conditional approval for the prospective IDE study to begin initially at 10 centers with 10 patients, while the company addressed some questions the FDA had found after reviewing the study design.

October 16, 2008 - Lumen Biomedical Inc. said that Principal Investigator Subbarao V. Myla, M.D., presented the results from the EPIC clinical trial — “Evaluating the Use of the FiberNet Embolic Protection System in Carotid Artery Stenting” — at TCT 2008.

From March 2007 to May 2008, the multicenter, single-arm EPIC clinical trial evaluated the FiberNet Embolic Protection System during carotid artery stenting of 237 high surgical risk patients with a critical carotid artery stenosis. The EPIC trial was an FDA IDE clinical study sponsored by Lumen Biomedical Inc.

October 16, 2008 - The one-year follow-up of the FAME study (FFR vs. angiography for multivessel evaluation) was presented at TCT 2008 and confirms the beneficial clinical and economic impact of FFR when used routinely to guide treatments of multi-vessel disease.

October 16, 2008 - At TCT 2008, Volcano Corp. launched its new PrimeWire Pressure Guide Wire, and the s5-FFR Option for its existing installed base of s5 and s5i imaging consoles in the U.S.

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