Spineart Announces FDA Approval of BAGUERA® C Cervical Disc
As one of Spineart's foundational technologies and a cornerstone of its cervical portfolio, BAGUERA® C brings nearly two decades of international clinical experience to a market with relatively few cervical disc replacement options. Since its introduction, over 80,000 devices have been sold worldwide, establishing a long track record of clinical use.
The FDA approval is supported by two randomized controlled trials with nearly 600 patients enrolled in
"This approval represents an important milestone for Spineart and for surgeons seeking an alternative to spinal fusion in appropriately selected patients," said
The addition of BAGUERA® C in
To learn more about BAGUERA® C, visit: https://www.spineart.com/us/solutions/baguera-c/
About Spineart
Spineart is a global fast-growing company in spine surgery innovation, dedicated to accelerating the adoption of cutting-edge technologies for surgeons and hospitals worldwide for the benefit of their patients. Renowned for its commitment to Quality, Innovation, and Simplicity, Spineart continues to push the boundaries of spinal surgery with its comprehensive portfolio of procedural solutions and digital technologies. Spineart was awarded the "Prix de l'Economie Genevoise 2022" for its contribution to technological and scientific innovations, commercial activities, job creations and ESG principles.
Please visit www.spineart.com and follow on LinkedIn.
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SOURCE Spineart
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