Exactech, a global medical technology leader, announced today it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Truliant® Porous Tibial Tray, a 3D tibial knee implant.
The Truliant Porous Tibial Tray leverages additive manufacturing technology to create a porous structure designed to mimic the structure of cancellous bone. This design aims to facilitate both initial and biological fixation, designed to accommodate patients’ active lifestyles.
“With a focus on cementless fixation and increased efficiency, it is no surprise that Truliant Porous is the fastest growing segment of Exactech’s knee portfolio,” said Exactech Chief Marketing Officer and Senior Vice President of Large Joints Adam Hayden. “By expanding our porous offerings with the laser-printed tray, knee surgeons will have access to additional sizing and fixation options for the personalization of their patients’ total knee replacement procedures, improving upon Exactech’s already successful cementless knee.”
Exactech’s Truliant Porous laser-printed 3D tibial tray features peripherally placed tibial pegs, a dual v-channeled keel and optional cancellous bone screws designed to increase initial rotational stability and allow an increased bone-implant interface.
This FDA clearance marks a significant milestone for Exactech, positioning the company to continue to address the growing demand for cementless knee solutions. More here.
