MOUNTAIN VIEW, Calif., Feb. 28 /PRNewswire/ -- Cardiva Medical, Inc., a privately held medical device company and developer of the Boomerang Catalyst(TM) System announces that it will present the highlights of the Boomerang Catalyst II System on February 29 at 9:20am at the Medtech Insight/Windhover Information's "Investment In Innovation (In3) West" medical technology investment and partnering conference held at The Venetian in Las Vegas, NV.
The Boomerang Catalyst II System builds on the success of its predecessor, the Boomerang Catalyst System, by adding an additional pro-coagulant to the proprietary hemostatic material of the Catalyst System. These generations are the first vascular closure devices to achieve final hemostasis on diagnostic patients in the catheterization lab leaving absolutely nothing behind in the patient, thereby eliminating a major source of complications, device failures, and re-access challenges. Additionally, clinical results presented in October 2007 at the TCT meeting in Washington D.C. showed that patients required statistically significantly less bed rest than patients utilizing the gold standard of manual compression for closure of the arterial access site.
To date, the family of Boomerang devices has been used in more than 100,000 percutaneous catheterization procedures in the U.S. During these procedures, a catheter is threaded through the femoral artery to the site of vascular disease (most common is in the heart), where diagnosis and/or treatment (such as stenting or angioplasty) can be performed. Traditionally, doctors have used two primary methods to close the femoral artery puncture site: direct manual compression over the puncture site or one of the various implantable vascular closure devices, which use materials (such as collagen, sutures, or staples) to create a physical seal of the puncture site.
"The Catalyst II device promises to build upon the already impressive
clinical achievements of its p
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