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Spineology Initiates Post-Market Lateral Interbody Fusion Study Using Novel Implant Design

ST. PAUL, Minn. – Spineology Inc., the innovator in anatomy-conserving spine surgery, has announced the initiation of a prospective, post-market lateral interbody fusion study designed to evaluate patient outcomes using its FDA-cleared Duo™ Lumbar Interbody Fusion System. The Duo System offers a unique implant design that is the first to combine PEEK, titanium, and graft containment mesh elements. The design dramatically reduces the access required to implant a device compared to traditional lateral systems. By minimizing the nerve and soft tissue retraction typically required in these surgeries, the company believes the Duo System can reduce the post-operative thigh pain and...


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