Zimmer Biomet’s Partial Knee System Gets FDA OK

Zimmer Biomet has obtained the FDA’s 510(k) clearance for its ROSA Partial Knee System, an imaging system designed for use in robotically assisted partial knee replacement surgeries.

Designed to be compatible with the company’s Persona Partial Knee implant system, the system is a component of Zimmer’s ZBEdge, a digital and robotic data-gathering platform.

The ROSA system features 2D to 3D imaging technology and real-time intraoperative data collection for soft tissue and bone anatomy to improve bone cut accuracy and analyze the range of motion.