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Spinal Fusion Devices Market Report, Analysis, Insights, Demand and Restraints up to 2025

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  Spinal Fusion Devices  Spinal fusion devices are used to stabilise a spine that has become unstable owing to a fracture, degenerative diseases of the spine, trauma, tumours, or deformity. A restricted blood supply, infections, traumas, and compression by a shattered bone or tumour are all common causes of spinal cord injury. According to Coherent Market Insights, The global spinal fusion devices market was valued at US$ 7,462.4 million in 2016 and is expected to witness a CAGR of 4.6% over the forecast period (2017 – 2025). The technology and mechanism of spinal fusion devices has advanced throughout time. Advanced plating methods increase structural stability and integrity. Innovative locking mechanisms and screw systems, which can have self-drilling and self-tapping characteristics, are used in spinal fusion devices. They are built of current manufacturing materials such as titanium alloy and have single and double holes per vertebrae through which the screw fixation is done.

Bone Graft Substitutes Are Becoming Popular Choice Of Surgeons As They Are Available In Several Different Types Catering Patients’ Requirements

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  Bone Graft Substitutes  Bone grafts have been used for years to fill in missing bones in the body. The process was first developed in the 19th century, however, is now a widely used surgery. About 10% of all orthopaedic and trauma surgeries result in a bone defect. Today, there are several different types of bone grafts available to surgeons. Some of these are more expensive than others, still the long-term results of these surgeries are well worth it. There are several types of bone graft substitutes available on the market. Traditional autologous bone grafting is one of the most commonly used options, and alternative bone grafting comes from the iliac crest or other local sources. There are six main categories of alternative bone implantation: nonstructural allograft, cadaver allograft, demineralized bone granules, synthetic bone granules, and autologous cellular gratings. Each of these products has a different regulatory pathway, and the data required to be published vary. Curre

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