SpineJack FDA Trial Completes Patient Enrollment

Vexim completed enrollment in its FDA clinical trial comparing SpineJack® to balloon kyphoplasty on 152 patients with osteoporotic vertebral compression fractures.

The 12-site prospective, randomized study is underway in France, Germany, Italy, Spain and Switzerland to support a planned FDA 510(k) submission by the end of 2017. Researchers...

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JV

Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.



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