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Clinical Experience Documenting Results • Since 2004, a prospective trial has been ongoing in Europe
that pools data from 9 evaluating centers to • Since 2003, a similar study is in progress for Mobidisc in treating lumbar degenerative disease. • In 2006, LDR was the first company to obtain FDA approval to conduct an IDE study for the Mobi-C for both one and two levels in the United States. • LDR is committed to helping surgeons, through national or international publications, to continually inform the worldwide community about our clinical results. International Training LDR also regularly engages leading surgeons to review
clinical results, assess the product performance, and make suggestions on how to
improve the surgical techniques. CAUTION: The Mobi-C™ artificial disc is an Investigational
Device and is limited to investigational use in the United States. The Mobi-L™ (Mobidisc®)
is not available in the United States. |
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