Wenzel Spine earns FDA clearance for new fusion device

Wenzel Spine earned FDA clearance for the PrimaLOK SP system, the devicemaker said Aug. 22.

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The device is designed for spinal fusion and can be used at multiple levels for patients with lumbar spinal stenosis, according to a news release. It has a locking mechanism for stabilization, high flexibility and is designed for minimal tissue disruption and improved radiographic visibility. 

“This achievement reflects our ongoing commitment to innovation and excellence in our spinal solutions,” CEO William Wilson said in the release. “We believe this system will significantly contribute to improved patient outcomes through a less invasive approach.”

At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 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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