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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