The company — set to be acquired by Zimmer Biomet — said that, on July 26, the first-ever fully autonomous, saw-based robotic ...

WARSAW, Ind., and ZURICH, Nov. 18, 2024/ PRNewswire/-- Zimmer Biomet Holdings, Inc., a global medical technology leader, today received the CE Mark for its Persona ® Revision Knee System.

The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's new revision knee implant component, Persona Revision SoluTion Femur, to provide an option for individuals ...

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 ...

Lucknow: Doctors at KGMU's department of orthopaedics successfully performed a partial knee replacement using the microplasty ...

Compared to traditional partial knee replacements that use bone cement to secure the implant in place, a cementless approach allows patients' natural bone growth to secure the implant for better ...

By Elise Reuter - Medcity News on November 08, 2020 11:00 am ...

Medtech firm Zimmer Biomet Holdings beat Wall Street estimates for first-quarter profit on Thursday, on the back of robust demand for its devices that are used in knee and hip reconstruction ...

The Zimmer Natural-Knee had been available for 25 years until its redesign. It includes a porous material that attaches to the bone without having to cut any of it away. The Natural-Knee II cruciate ...

--Zimmer Biomet Holdings, Inc., a global leader in musculoskeletal healthcare, today announced U.S. Food and Drug Administration 510 clearance of the ROSA ® Partial Knee System for robotically ...

WASHINGTON (CBS.MW) -- Zimmer Holdings said Wednesday that it has launched a unique implant for patients who need partial knee replacement and also are capable of high degrees of joint movement.