Prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of the ProDisc-L total disc replacement compared with circumferential arthrodesis for the treatment of two-level lumbar degenerative disc disease: results at twenty-four months. [electronic resource]
- The Journal of bone and joint surgery. American volume Apr 2011
- 705-15 p. digital
Adult Arthroplasty, Replacement--instrumentation Device Approval Disability Evaluation Female Humans Intervertebral Disc Intervertebral Disc Degeneration--complications Low Back Pain--etiology Lumbar Vertebrae--surgery Male Pain Measurement Patient Satisfaction Postoperative Complications Prospective Studies Prostheses and Implants Prosthesis Design Range of Motion, Articular Recovery of Function Spinal Fusion--instrumentation Statistics, Nonparametric Treatment Outcome United States United States Food and Drug Administration