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Clinical Experience  

Documenting Results
LDR’s reputation escalated as word
of its new developments and strong
clinical performances in Europe
circulated. Demonstrating this strong
clinical performance is critical to the
ongoing success of LDR’s products.

• Since 2004, a prospective trial has
been ongoing in Europe that pools
data from 9 evaluating centers to
assess the safety and efficacy of
the Mobi-C in treating cervical
degenerative disease.

• 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 created a well-organized and utilized international training program where interested doctors from all over the world are brought to the experts in their home country. In this hands-on learning environment, the expert surgeon can share their experience and surgical technique with maximum effectiveness.

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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