The Global Cervical Total Disc Replacement Device Market, by Material ( Metal over Metal and Metal over Biocompatible), by Design (Constrained, Semi-constrained, and Unconstrained), by End User ( Hospitals, Ambulatory Surgical Centers, and Clinics) and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) was valued at US$ $ 771.6 million in 2017, and is projected to exhibit a CAGR of 22.1% over the forecast period (2018 – 2026), as highlighted in a new report published by Coherent Market Insights.
The Cervical Total Disc Replacement (C-TDR) device is used in patients diagnosed with degenerative disc disorders. Neck pain and cervical radiculopathy are the major symptom of degenerative disc disorders in the cervical region of the spine. Artificial disc placement surgery is performed when no other treatment works for patient. In this degenerated disc is removed surgically and an artificial disc is implanted in the vertebra. Key players in the market are providing training to spine surgeons to ensure the efficient handling of their respective products. Major factors driving growth of the global cervical total disc replacement device market are increased prevalence of degenerative disc disorders and chronic pain among population. Cervical radiculopathy and myelopathy secondary to cervical degenerative discs are common diagnoses in adult patients. It causes disability and loss of productivity with reduces quality of life. According to data published by American Associated of Neurological Surgeons given, in 2016, more than around 200,000 cervical surgical procedures are performed in the U.S. Aging population is prone to cervical disc disorder and cervical spondylitis, which is fueling growth of the market.
Key players are launching innovative products to address clinical need of cervical total replacement device, which in turn is propelling growth of the global cervical total disc replacement device market. In April 2018 – DePuy Synthes (Part of Johnson & Johnson Medical Devices Companies) U.S. launched its PROTI 360° Integrated Titanium Family of spinal fusion devices (artificial cervical and lumbar disc) for treatments of patients suffering from degenerative disc disease in the neck and back. It is the only titanium-integrated polyetheretherketone (PEEK) that offers 360 degrees of titanium integration therefore it offers combine benefits of PEEK and titanium (forms a bioactive surface which promotes the attachment and growth of bone-forming cells) and allows to observe bone healing process. In January 2018, NuVasive, Inc. received the FDA 510(k) clearance for expanded indications of COHERE cervical interbody fusion device. Furthermore, COHERE received a new ICD code from the Center of Medicare & Medicaid Services (CMS) in October 2017
Browse 45 Market Data Tables and 35 Figures spread through 200 Pages and in-depth TOC on “Cervical Total Disc Replacement Device Market - by Material (Metal over Metal and Metal over Biocompatible), by Design (Constrained, Semi-constrained and Unconstrained), by End User (Hospitals, Ambulatory Surgical Centers and Clinics), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) - Global forecast to 2026”
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Companies are conducting and publishing clinical trials for artificial cervical disc in order to create edge over other treatment approaches such as anterior cervical discectomy and fusion. For instance Globus Medical, Inc. published seven year clinical trial data in 2017, which demonstrated superior results with its Secure C cervical artificial disc over anterior cervical discectomy and fusion. In March 2018, Zimmer Biomet Holdings, Inc. announced and published the full seven-year follow-up data from a study evaluating the Company's Mobi-C Cervical Disc for total disc replacement.
Key players are undertaking strategic collaboration in order to expand their product offering and geographic presence in different regions across the globe. In September 2017, NuVasive, Inc. acquired Vertera Spine, which is medical device company that develops and commercialize innovative interbody implants for spinal fusion using patented porous polyetheretherketone (PEEK) technology. With this acquisition NuVasive is currently the only medical device company to offer porous interbody technology across both PEEK and titanium materials, thereby addressing orthopedic surgeons’ needs and choice for interbody implants. Globus Medical, in 2016, acquired international operations and distribution channels of Alphatec Holdings, Inc. It would allow Globus access to Japan and increased presence and penetration in other key regions.
Key Takeaways of the Cervical Total Disc Replacement Devices Market:
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