Warsaw-based Zimmer Biomet, a global medical technology leader, today announced U.S. Food and Drug Administration, clearance ...
Zimmer Biomet announced today that the FDA granted 510(k) clearance for its Rosa Knee surgical robot with OptimiZe technology ...
Medical Device Network on MSN
Zimmer Biomet secures FDA approval for ROSA Knee with OptimiZe system
The system helps surgeons deliver personalised and consistent outcomes during robotic-assisted total knee replacement ...
Knee replacement surgery effectively addresses severe knee conditions like osteoarthritis, offering pain relief and improved mobility. The procedure sees high demand due to rising osteoarthritis among ...
Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global medical technology leader, today announced U.S. Food and Drug ...
"For younger and more active patients, the Oxford Cementless Partial Knee amplifies the benefits of a traditional partial knee replacement by offering knee flexion that resembles natural knee movement ...
Noblesville-based Indiana Orthopedic Institute is an early adopter of a “cementless” partial knee replacement system recently launched in the United States but has long been used in Europe and ...
-- New Porous Iteration of Anatomic Keeled Tibia Designed to Deliver Stable Initial and Biological Fixation Together with the Clinically Proven Benefits of the Persona Knee System -- "With an ...
Knee replacement lawsuits typically claim the devices loosened, became unstable and required revision surgery, according to a report from Drug Watch. 1. Devices like DePuy Attune, Zimmer NexGen, and ...
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