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How would you characterize patients’ experience with the Menaflex device?

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How would you characterize patients’ experience with the Menaflex device?

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The Menaflex device has been implanted in more than 2,500 patients in Europe and 162 patients in the United States. Surgeons have documented successful results involving Menaflex procedures through a number of scientific presentations and publications, and demand for the device is on the rise. Patients report positive experiences with the device, which has an excellent safety record. The Menaflex originally was approved for use in Europe in 2000, and now is used in 10 countries (Austria, Belgium, Germany, Italy, Poland, Spain, South Africa, Switzerland, Turkey and the United Kingdom). More than 400 surgeons have been trained to use the device outside the United States. In the United States, the Menaflex was the subject of a multicenter clinical trial conducted at 16 centers involving 25 surgeons. The device was cleared by the FDA for sale in the United States in December 2008. U.S. surgeon training is underway, and ReGen plans to begin immediate U.S. commercial distribution of the Mena

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