The FDA granted the Bone Bolt System a 510(k) clearance to sell and market the device in the U.S. This milestone marks the first time that a novel medical device has received an FDA 510(k) clearance in University of Utah’s history.
“As one of the nation’s leading research universities, innovation plays a central role in our mission to improve the quality of life of our patients—OIC’s Bone Bolt System does just that,” said University of Utah President Taylor Randall. “Not only will the device make a difference in the care we can provide at University of Utah Health, but it illustrates our commitment to turn research into real-world impact by getting it to market as soon as possible, to improve health outcomes more broadly.”