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]
Producer: 20110726Description: 705-15 p. digitalISSN:- 1535-1386
- 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
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Publication Type: Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
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