TA Criterion 1: The technology must have final approval from the appropriate government regulatory bodies. The Prestige® Cervical Disc (Medtronic Sofamor Danek, Memphis, TN) received FDA Premarket ...
UCSF Spine Center surgeons are conducting a clinical trial to investigate the safety and effectiveness of an implant that replaces damaged discs in the neck. The trial will compare the implant to ...
The FDA recently approved the Medtronic Prestige LP Cervical System for treating degenerative disc disease at two adjacent vertebral levels (between C3 and C7). The device is said to be Medtronic’s ...
A recent assessment by the BCBSA TEC in August 2009 found that the use of "artificial intervertebral disc arthroplasty for the treatment of patients with cervical degenerative disc disease does not ...
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