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
Zimmer Biomet’s G7 is our acetabular system, specifically designed to simplify implant and instrument delivery, optimise operative efficiency, and improve clinical performance Watch this video and discover more about G7 Acetabular system. Click here when you are ready to see more: 👉 https://www.zimmerbiomet.eu/en/products/g7-r-acetabular-system This video is intended for Healthcare professionals in the EMEA region only.
Written by Zimmer Biomet on YouTube.
