According to the registry data, 10% (14,216 of 142,550) of TKAs performed during this study period used robotic assist. According to the research team, there was no statistically significant change in ...

Zimmer Biomet has scored an FDA clearance for a new component of its total knee replacement offering, aimed at patients who may be sensitive to certain metals or bone cement. The Persona SoluTion ...

“With the FDA clearance of Persona SoluTion PPS Femur, in combination with our Persona OsseoTi ® Tibia and OsseoTi Patella, we are proud to offer surgeons a fully cementless alternative to ...

The Persona SoluTion PPS Femur features a porous coating for cementless fixation and leverages a proprietary surface treatment designed to enhance wear performance.1,2 "With the FDA clearance of ...

WARSAW, Ind. - Zimmer Biomet Holdings, Inc. (NYSE:ZBH), a global leader in medical technology, announced today the U.S. Food and Drug Administration (FDA) has granted Premarket Approval for its ...

The approval is based on safety and effectiveness data from an Investigational Device Exemption (IDE) study and non-clinical testing for cementless partial knee replacement (PKR).1 The Oxford ...