Natural design. Amplified: Smith+Nephew announces FDA 510(k) clearance and first surgical cases of LANDMARK™ Total Knee System

Summary by AI BETAClose X

Smith+Nephew has received FDA 510(k) clearance for its LANDMARK Total Knee System, a next-generation knee replacement designed to replicate natural knee anatomy and motion, and has successfully completed initial surgical cases. This system is engineered to work with CORI KNEE Handheld Robotics Arthroplasty, offering a personalized approach to total knee arthroplasty. The LANDMARK Knee features a fully 3D-printed femoral component utilizing CONCELOC Technology and is designed for improved patella tracking. Commercial introduction will be phased, with broader availability expected by 2027.

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