FDA 510(k) for Corin Apollo Robotic-Assisted Total Knee Arthroplasty

Corin received FDA 510(k) clearance for its Apollo Robotic-Assisted Surgical platform and the ApolloKnee software application.

Corin’s experience in robotic-assisted total knee arthroplasty began with its OMNIBotics technology. The Apollo platform, with BalanceBot technology, builds upon a decade of clinical success to focus on future enhancements in patient outcomes while providing an intuitive experience for surgeons.

Now, the Apollo platform technology is slated to expand Corin’s capabilities into additional clinical applications across joint arthroplasty in the coming years.

Source: Corin Group