[iSpine Admin]

2007:

• Fentanyl Advisory

• ProDisc-C Receives FDA Approval

• FDA Approvable Letter Received

• Effect of uncovertebral joint excision on the motion response of the cervical spine after total disc replacement

• Comparative charge analysis of one- and two-level lumbar total disc arthroplasty versus circumferential lumbar fusion.

• The ability of diagnostic spinal injections to predict surgical outcomes

• The accuracy and validity of "Routine" X-rays in estimating lumbar disc arthroplasty placement

• In vivo evaluation of dynamic characteristics of the normal, fused, and disc replacement cervical spines

• Bryan artificial cervical disc arthroplasty in a patient with Klippel-Feil syndrome

• Acquired spondylolysis after implantation of a lumbar ProDisc II prosthesis

• An economic model of one-level lumbar arthroplasty versus fusion

• The ProDisc-C prothesis - Clinical and radiological experience

• Significantly improved lumbar arthroplasty placement using image guidance

• Posterior avulsion fracture at adjacent vertebral body during cervical disc replacement with ProDisc-C - A case report

• Comparison of biomechanical function at ideal and varied surgical placement for two lumbar artificial disc implant designs - Mobile-core Versus fixed-core

• Total lumbar disc replacement in athletes: clinical results, return to sport and athletic performance

• Range of motion change after cervical arthroplasty with ProDisc-C and Prestige artificial discs compared with anterior cervical discectomy and fusion

• Survival and clinical outcome of SB Charite III disc replacement for back pain

• Revision open anterior approaches for spine procedures

• Results of the prospective, randomized, multicenter FDA investigational device exemption study of the ProDisc-L total disc replacement versus circumferential fusion for the treatment of 1-level degenerative disc disease

• Total lumbar disc replacement: different results for different levels

• Revision and explantation strategies involving the CHARITE lumbar artificial disc replacement

• Long-segment fusion of the thoracolumbar spine in conjunction with a motion-preserving artificial disc replacement

• CHARITE versus ProDisc - A comparative study of a minimum 3-year follow-up

• Long-term results of one-level lumbar arthroplasty: minimum 10-year follow-up of the CHARITE artificial disc in 106 patients

• US Clinical Trial Procedures Underway

• Magnetic resonance imaging clarity of the Bryan, Prodisc-C, Prestige LP, and PCM cervical arthroplasty devices

• Disc replacement using Pro-Disc C versus fusion: a prospective randomised and controlled radiographic and clinical study

• Release of cobalt and chromium ions into the serum following implantation of the metal-on-metal Maverick-type artificial lumbar disc (Medtronic Sofamor Danek)

• Early removal of a Maverick disc prosthesis

• Polyethylene wear and rim fracture in total disc arthroplasty

• Prevalence of heterotopic ossification following total disc replacement

• Polyethylene wear debris and long-term clinical failure of the Charité disc prosthesis