FDA Clears Binder Biomedical’s LOGIC Spinal Fusion Device

The U.S. FDA recently approved Binder Biomedical’s LOGIC standalone intervertebral body fusion device for treatment of degenerative disc disease.

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The LOGIC system was crafted for use in direct anterior surgical approach of the lumbar spine. The national launch will take place in the fourth quarter of 2014.

The device is made out of PEEK-OPTIMA, the proprietary polymer from Invibio Biomaterial Solutions.

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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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