Please provide your email address to receive an email when new articles are posted on . Zimmer Biomet received FDA premarket approval for its Oxford cementless partial knee replacement implant. The ...

That’s the question facing orthopedic surgeons and rehab physicians as they learn to work with a new knee replacement that incorporates sensors and processors to send data about how the joint works ...

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 ...

"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 ...

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 ...

CHICAGO, July 14 (Reuters) - Orthopedic device maker Zimmer Holdings Inc on Monday said it notified U.S. health regulators that is recalling a surgical instrument used in implanting its NexGen ...

On Wednesday, Zimmer Biomet Holdings, Inc (NYSE:ZBH) reported third-quarter adjusted EPS of $1.74, up from $1.65 a year ago, in line with the Street estimates. The orthopedic giant reported sales of ...

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 ...