Kiva Device for Spinal Fractures Cleared by FDA

The Kiva VCF Treatment System by Santa Clara, Calif.-based Benvenue Medical has received FDA 510(k) clearance for the treatment of spinal fractures.

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The Kiva system is an implant-based treatment for vertebral augmentation and an alternative to balloon kyphoplasty. The cylindrical implant is made of PEEK-OPTIMA material.

The results of the Kiva safety and effectiveness trial will be presented at the upcoming Society for Interventional Radiology meeting in March.

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At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 18–20 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

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