www.fdanews.com/articles/200986-depuy-synthes-earns-fda-clearance-for-knee-replacement-robotic-assistance-platform
DePuy Synthes Earns FDA Clearance for Knee-Replacement Robotic-Assistance Platform
January 22, 2021
The FDA has given 510(k) marketing clearance for Johnson & Johnson (J&J) subsidiary DePuy Synthes’ VELYS Robotic-Assisted Solution, a device that helps surgeons with total knee replacements.
The table-mounted robotic platform is designed to be used with J&J’s ATTUNE Total Knee System to support surgeons in planning and performing surgeries for total knee replacement.
The system does not require pre-operative imaging to accurately resect bones and position knee implants, and offers advanced planning capabilities, the company said.