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Stryker Gains FDA Clearance for SpineJack Fracture Reduction -

Stryker received FDA 510(k) clearance to market the SpineJack® implantable reduction system to treat osteoporotic vertebral compression fractures. Limited launch will occur throughout the end of 2018. SpineJack comprises three titanium implants of differing diameters that address 95% of VCFs and all patient morphologies. The 30-minute, minimally invasive x-ray guided procedure is intended to support patient discharge shortly after surgery. (Stryker Corp., 9/26/18)