|Eden Spine's Vertebral Body Replacement receives CE Mark Approval|
Monday, December 20th, 2010 - 9:00 am ET
Lake Mary, Florida Eden Spine (www.EdenSpine.com) a Florida based Medical Devices organization announced today that the GIZA™was granted CE Mark approval.
“The GIZA™ is a new generation VBR, specifically designed to save valuable O.R. time and decrease the risk of subsidence,” says Mourad Ben Mokhtar head of Eden Spine’s research and developments efforts.
The technology is intended to replace and fuse a collapsed, damaged, or unstable vertebral body due to a tumor or a fracture. It is a reliable and intuitive system for one or two level fusions.
“With its CE Mark,” added Guillaume Viallaneix, CEO, “the GIZA™ is available for international distribution. US market approval is expected during the first half of 2011.”
###Eden Spine is headquartered in the United States, with a wholly owned subsidiary in Geneva, Switzerland. The Eden Spine Group is positively impacting patient care and creating substantial value developing tomorrows’ spinal technologies and building a world class spine franchise, inclusive of a fiscally responsible US and OUS sales & distribution network. The organization is commercially active in the United States, Europe, the Middle East and Latin America. The company possesses a deep portfolio of spinal technologies including three new-generation motion preservation technologies; the WELLDISC™ total disc replacement; the PERFX-2™ Dynamic Stabilization System, and the WELLEX™ Interspinous Technology. Eden Spine distributes a range of FDA-cleared and CE Marked spine technologies in the US and internationally.
Guillaume Viallaneix, CEO, Phone: Phone: 407-792-2279 - Fax: 407-264-8303 - e-mail: CLOAKING
Headquarters: Eden Spine, LLC - 801 International Parkway - 5th Floor - Lake Mary, FL 32746 - USA
International: Eden Spine Europe SA - Bd Helvetique, 36 - 1207 Geneva- Switzerland
Web address: http://www.EdenSpine.com