SpineGuard Release: Study Shows Use of PediGuard® Reduced the Incidence of Clinically Relevant Misplaced Pedicle Screws in Spine Surgery

SAN FRANCISCO & PARIS--(BUSINESS WIRE)--SpineGuard® announced today that the third published clinical study of its FDA-cleared and CE-marked PediGuard® platform for enhanced pedicle screw placement has concluded that “the use of PediGuard significantly reduced the incidence of clinically relevant misplaced screws, thereby increasing the safety of pedicle screw implantation*.” Principal investigator for the study was Dr. Dror Ovadia, Department of Pediatric Orthopaedics, Dana Children’s Hospital, Tel Aviv, Israel. The study has been published in the September 15 issue of the peer-reviewed medical journal Spine.

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