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Home » DePuy Synthes Earns FDA Clearance for Knee-Replacement Robotic-Assistance Platform
DePuy Synthes Earns FDA Clearance for Knee-Replacement Robotic-Assistance Platform
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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.
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