What Is Cervical Disc Replacement

Artificial Cervical Disc Arthroplasty (or Cervical Disc Replacement) is an FDA approved surgical procedure that removes damaged or degenerated cervical disc and replacing it with an artificial disc device. Cervical discs serve as cushions or shock absorbers between the vertebra of the neck (cervical spine). Cervical discs degenerate or get worn out due to trauma and aging, which can be source of neck pain and cause other neurologic symptoms, such as numbness or weakness that radiates from the neck into the arms. Displaced or damaged disc can cause pressure on the central spinal cord or on the individual nerve roots that exit from the spinal canal. If left untreated, damaged disc causes the formation of bone spurs, also called osteophytes, which can also cause pressure on the spinal cord or nerve roots.

Dr Robert Jackson was a principal investigator and surgeon in the FDA research trial to get cervical disc replacement approved in the United States.  He has been doing cervical disc replacements since 2007, and has taught numerous courses to surgeons on the techniques of cervical disc replacement and cervical fusion surgery.

Mobi-C® Artificial Cervical Disc Replacement

Mobi-C® artificial cervical disc has been designed to restore segmental motion and disc height in the neck region. The Mobi-C® cervical disc is indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following discectomy at one level or two contiguous levels for intractable radiculopathy (arm pain and/or a neurological deficit) with or without neck pain, or myelopathy due to abnormality localized to the level of the disc space and at least one of the following conditions confirmed by radiographic imaging (CT, MRI, X-rays): herniated nucleus pulposus, spondylosis (defined by the presence of osteophytes), and/or visible loss of disc height compared to adjacent levels. The Mobi-C® artificial cervical disc is implanted using an anterior approach. With anterior cervical discectomy technique, an incision is made in the front of the neck which allows the surgeon to remove the damaged disc and bone spurs to relieve any pressure on the spinal cord and nerve roots and implant the artificial cervical disc.

Patients should have failed at least 6 weeks of conservative treatments or demonstrated progressive signs or symptoms despite nonoperative treatment prior to implantation. Standard treatments for cervical disc disease usually involve non-surgical options such as physical therapy, medications and spinal injections.

Facts About Mobi-C® Cervical Disc:

  • FDA approved for use in the US in August 2013
  • First implantation was completed in November 2004 in France
  • Designed by an experienced French surgeon team
  • Features patented mobile bearing technology
  • Provides a bone sparing technology
  • Specially designed for optimal positioning