Aurora Spine’s ZIP Fusion System Receives FDA 510(k) Clearance

Aurora Spine has been granted FDA 510(k) clearance for its ZIP minimally invasive interspinous fusion system.

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The ZIP system was designed to be a pedicle screw alternative. It has already launched in Europe and will immediately launch in the U.S. with its new approval. Aurora Spine has 35 U.S. distributors for ZIP sales.

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