Ankle Fusion Nail Industry: Uptake of Global Ankle Fusion Nail Increasing Worldwide

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The global ankle fusion nail market has seen significant growth in the last five years with the development and approval of new minimally invasive fusion devices.

Global Adoption of Minimally Invasive Ankle Fusion Nail Industry Technology

The global ankle fusion nail market has seen significant growth in the last five years with the development and approval of new minimally invasive fusion devices. Ankle fusion nails allow surgeons to perform ankle arthrodesis through a smaller incision compared to traditional plate techniques, reducing surgical trauma and improving post-operative recovery.

Several factors have driven the increased utilization of Ankle Fusion Nail. The benefits of minimally invasive surgery such as less soft tissue dissection, reduced blood loss, and faster rehabilitation are well recognized by both patients and surgeons. The availability of user-friendly ankle fusion nails from major orthopedic manufacturers has also expanded adoption outside of large academic centers.

Another factor is the rising prevalence of ankle arthritis due to an aging population as well as increased rates of high ankle sprains and complex ankle fractures resulting from more high-impact sports and work injuries. While triple arthrodesis remains the gold standard treatment for advanced ankle osteoarthritis, minimally invasive ankle fusion with intramedullary fixation has become a viable alternative for suitable candidates.

Regulatory Approvals of New Devices Spur Ankle Fusion Nail Industry

Over the last five years, three new ankle fusion nail systems have received regulatory approvals in Europe, Canada, and the United States, expanding options for surgeons.

In 2017, Zimmer Biomet received CE Mark and Health Canada approval for its PROPHECY Pre-Contoured Ankle Fusion Nail. Unique features of PROPHECY include a pre-contoured nail shape for anatomical fit and a proprietary interlocking screw design said to reduce the risk of screw backout compared to conventional designs.

Stryker Orthopaedics obtained US FDA clearance for its T2 Ankle Fusion Nail in early 2020. The T2 system utilizes a novel intra-operative bending function allowing surgeons to contour the nail during surgery for optimal fit in complex ankle deformities. Additionally, its dynamic interlocking screw technology is designed to maximize construct stability.

Most recently in late 2021, Wright Medical gained US and European approval for its In balance Ankle Fusion Nail. Key attributes of In balance include a variable angle locking bolt insertion aimed at simplifying placement and a threaded distal aperture claimed to promote fusion. Early clinical results have demonstrated fusion rates comparable to traditional methods.

Rising Asian Markets Drive Global Sales Growth

While the major orthopedic markets in North America and Europe continue to see steady uptake of minimally invasive ankle fusion technology, some of the highest growth rates over the next five years are projected to occur in Asia. Rapid urbanization and aging of populations in China, Japan, and South Korea are fueling increases in degenerative ankle conditions treatable with arthrodesis.

In China alone, the increasing incidence of ankle osteoarthritis along with rising income levels are expected to support over 15% annual growth of the ankle arthrodesis device market through 2027 according to a recent market analysis. Local manufacturers as well as global companies are working to address this demand through regulatory registrations, investments in sales and training infrastructure, and joint venture partnerships.

Japanese and South Korean payers have also demonstrated growing reimbursement for innovative ankle fusion technologies. The ability to perform arthrodesis through a smaller incision with potentially shorter hospital stays and faster return to work has incentivized both private insurers and national health authorities to provide coverage for minimally invasive intramedullary devices. With aging populations and emphasis on both clinical efficacy and cost effectiveness, ankle fusion nail procedures are poised for continued expansion in these Asian markets.

Future Outlook - Biologics, Navigation, and Specialized Implants

Looking ahead, several pipeline products aim to further improve ankle fusion outcomes:

- Bone graft substitutes and growth factors are in development to enhance fusion rates without needing an autograft harvest. These biologics could decrease operative time and morbidity.

- Image-guided navigation platforms are undergoing clinical studies for ankle arthrodesis. When integrated with fusion nails, navigation may provide more accurate nail placement and predictable correction of deformities.

- Niche indications such as pilon fractures with ankle arthritis or tibiotalar dislocations may see adoption of specialized anatomically shaped fusion nails designed for complex reconstruction cases.

  • Long-term clinical data will be important to demonstrate whether minimally invasive ankle fusion can match the longevity of traditional techniques. Ongoing registries and investigations should continue to report on survivorship.

In summary, global adoption of ankle fusion nail technology appears poised for continued expansion through approvals of new devices, growth in Asia markets, and future innovation. Minimally invasive ankle arthrodesis brings clinical and economic benefits that will support increasing utilization worldwide.

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Author Bio:

Money Singh is a seasoned content writer with over four years of experience in the market research sector. Her expertise spans various industries, including food and beverages, biotechnology, chemical and materials, defense and aerospace, consumer goods, etc. (https://www.linkedin.com/in/money-singh-590844163)

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