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 ...
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 ...