ALTIOR TRAUMA ANNOUNCES FDA 510(K) CLEARANCE FOR THE ARTEMIS PROXIMAL FEMORAL NAIL SYSTEM (press release)
A FOURTH-GENERATION HIP FRACTURE NAIL MANUFACTURED USING A REVOLUTIONARY PROCESS
Altior Trauma, a GLW, Inc. company, (“Altior Trauma”) announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration for its Artemis Proximal Femoral Nail System (the “Artemis System”), a hip fracture nail. The Artemis System offers an advancement in hip fracture treatment that combines the strength of titanium with a unique blend of Solvay Zeniva® carbon fiber ...
