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Knee+ NexSight just received FDA 510(k) clearance!

Knee+ NexSight just received FDA 510(k)

We’re proud to share that our new handheld augmented reality guidance for TKA has received FDA 510(k) clearance, a meaningful milestone in our journey.

Built on our new platform and designed with efficiency in mind for ASCs and high-volume surgical environments, this step brings us closer to making AR navigation more accessible in everyday orthopedic practice.

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