Zimmer Biomet Holdings Inc. announced it received FDA 510(k) clearance for the Persona Revision Knee System. According to a company press release, Zimmer Biomet plans to launch the system in the ...
Add Yahoo as a preferred source to see more of our stories on Google. The system offers a simplified user interface Zimmer Biomet has received 510(k) clearance from the US Food and Drug Administration ...
Zimmer Biomet received a 510(k) clearance from the FDA for its robotic assistance platform for total knee replacement surgeries. The Rosa knee system includes three-dimensional, preoperative planning ...
WARSAW, Ind., April 20, 2021 /PRNewswire/ -- Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, today announced U.S. Food and Drug Administration 510(k) ...
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 ...
Total knee replacement surgery just got a bit of an IQ boost. The FDA offered up a de novo clearance for Zimmer Biomet and Canary Medical’s Persona IQ system, marking it as the first “smart” knee ...
Zimmer Biomet Holdings Inc. has won the FDA’s nod for its Rosa Partial Knee system for robotically assisted partial knee arthroscopy. The new system is the latest addition to the Rosa Robotics ...
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