cervical spinal fusion

cervical spinal fusion

surgery to relieve severe neck pain, as well as pain in shoulders, arms, and hands, caused by abnormal movement or adjustment of adjacent vertebrae, a pinched nerve, or spinal compression. The adjacent vertebrae are joined with metal devices and/or a bone graft made from human bone or a ceramic material. An anterior or posterior surgical approach may be used.
References in periodicals archive ?
com)-- Hoag Memorial Hospital Presbyterian is the first hospital in Orange County to offer a newly approved alternative to cervical spinal fusion - and the first patient to undergo the procedure, a woman in her mid-40s who suffered from debilitating neck pain and upper extremity numbness, was up and walking within hours afterward.
Mesoblast Chief Executive, Professor Silviu Itescu, said that cervical spinal fusion is a major commercial opportunity for Mesoblast.
More recently, the versatile polymer has been increasingly used in cervical spinal fusion devices, as evidenced by Alphatec's Novel Cervical Interbody device and others.
In a long-term follow-up study evaluating clinically relevant adjacent level degeneration following cervical spinal fusion, Hilibrand and colleagues demonstrated that symptomatic adjacent segment disease may affect more than one-fourth of all patients within ten years after cervical arthrodesis, as defined by the presence of new radiculopathy or myelopathy referable to an adjacent motion segment.
Following this pilot study, which was completed three months ahead of schedule, Orthovita will now begin an expanded pivotal study as a component of ongoing clinical trials to measure the safety and effectiveness of RHAKOSS for patients undergoing cervical spinal fusion surgery.
No Profile, Integrated Interbody system for anterior cervical spinal fusion procedures.
The Company's spinal bony fusion product NeoFuse(TM), currently in the midst of Phase 2 trials in the United States, has the potential to become a major revenue driver for the company since over 500,000 lumbar and cervical spinal fusion procedures are currently performed annually in the United States alone.
Food and Drug Administration (FDA) has granted an investigational device exemption (IDE) to conduct a clinical trial to study INFUSE(r) Bone Graft in a cervical spinal fusion.
The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), spondylolisthesis, trauma (i.
New applications for the devices, particularly for cervical spinal fusion, are also growing the industry.
ST01 is an artificial bone substitute material for lumbar, thoracic and cervical spinal fusion and related procedures.
The most common form of surgery for treating cervical degenerative disc disease is cervical spinal fusion, which is intended to relieve an impingement on the spinal cord or nerve root and relieve associated arm and/or neck pain.