Exactech announced today that it received FDA 510(k) clearance for its Truliant porous tibial tray, a 3D tibial knee implant.

Exactech, a global medical technology leader, announced today it has received 510(k) clearance from the U.S. Food and Drug ...

The implant utilises additive manufacturing techniques to create a porous structure that resembles a cancellous bone structure.

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 ...

Discover Exactech's latest innovation in knee replacement surgery with the FDA clearance of Truliant Porous Tibial Tray, featuring advanced 3D technology.

Methods: The treatment options for tibial plateau bone defects were classified into four categories: no treatment, cancellous bone filling, bone cement filling, and the cement-screw technique.

A possible explanation may be that the lag screws did not absorb the entire axial load force and transmit it to the cancellous bone. Instead, the additional abutment of the jail screw transmitted ...

The U.S. Food and Drug Administration (FDA) has granted 510 (k) clearance to a standalone lateral lumbar interbody fusion ...

EDTA was replenished regularly. To facilitate the absorption of EDTA into the cancellous bone in the vertebral body's center, 3 mm diameter holes were drilled at the pedicle on both sides. EDTA was ...