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Wednesday, October 20, 2021

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Zimmer Biomet Holdings

ROSA® Hip System FDA Cleared Reports Zimmer Biomet

ROSA Hip is designed for compatibility with multiple implant systems, including the Avenir Complete® Hip System, an evolution of the Avenir® Hip Implant that has a clinically-proven heritage of over 10 years.

ROSA® Knee System for Robotically-Assisted Surgeries Receives FDA Clearance

1/25/19: ROSA Knee is a robotically-assisted surgical system designed to help surgeons in performing total knee replacement surgery with features to assist with bone resections as well as assessing the state of soft tissues to facilitate implant positioning intraoperatively.

Zimmer Biomet Launches Mobi-C® Cervical Disc Replacement in Japan

9/17/18: The launch follows receipt of regulatory approval from the Japan Ministry of Health, Labour and Welfare (MHLW) in May 2018 and the receipt of reimbursement from the MHLW in June 2018. The first Mobi-C surgery in Japan was performed in July 2018. The Mobi-C Cervical Disc is a leading option for cTDR designed to restore a healthy disc height and maintain patient range of motion at the operated level.

Zimmer Biomet Announces 510(k) Clearance for Zyston® Strut Open Titanium Interbody Spacer System

5/23/18: "The Zyston Strut Open Titanium Interbody Spacer System is available in straight and curved profiles and is uniquely designed to provide surgeons with an option that optimizes the balance of strength and graft capacity in spinal fusion cases," said board certified orthopaedic surgeon Frank Schwab, MD, New York, NY. "I have worked with a variety of Zimmer Biomet's spine products and am looking forward to offering my fusion patients this latest innovation."

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