OrthoSensor Earns Further 510(k) Clearance

June 11, 2018

The FDA granted OrthoSensor, a developer of sensor-assisted devices for total knee replacement, additional 510(k) clearance for its Verasense assisted technology.

The device addresses dissatisfaction from patients regarding their total knee replacement surgeries, who complain of stiffness, pain and loss in range of motion.

The clearance allows the device to be used with Zimmer Biomet’s Persona knee system for total knee replacement.

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