DePuy bags FDA 510(K) clarence for robotic-assisted knee surgery device
The clearance for unicompartmental knee arthroplasty follows a previous clearance for the device in total knee arthroplasty.The post DePuy bags FDA 510(K) clarence for robotic-assisted knee surgery device appeared first on Medical Device Network.
The post DePuy bags FDA 510(K) clarence for robotic-assisted knee surgery device appeared first on Medical Device Network.
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