Against the record
ROSA, from Zimmer Biomet, is at stage 5 of 5 on our ladder: regulator-cleared or mass market. Cleared where approval applies, or widely sold. The latest milestone on its record is from 24 Jan 2019: The FDA cleared the ROSA Knee System through the 510(k) route (K182964). The application was filed by Orthosoft, a Zimmer Biomet company.
This video comes from the maker's own channel, and makers show their robots at their best. The stage above comes from dated public records, not from the video.
From the video's description
Calling all shoulder surgeons! Explore our Comprehensive Shoulder System now: https://www.zimmerbiomet.eu/en/comprehensive-shoulder-system-choose-zb The Zimmer Biomet YouTube page is informational only. For indications, contraindications, warnings, precautions, potential adverse effects and patient counselling information, see the package insert or contact your treating physician, or visit www.zimmerbiomet.eu. Not all patients are candidates for a Zimmer Biomet product and/or procedure. Only a medical professional can determine the treatment appropriate for your specific condition. Material posted to YouTube is not for distribution in France – for our full disclaimer please visit www.zimmerbiomet.eu.…
Written by Zimmer Biomet on YouTube.
