OrthoSensor’s VERASENSE Knee System Receives 510(k) Clearance

Sunrise, Fla.-based OrthoSensor received FDA 510(k) clearance for its VERASENSE knee system, an instrument system for implant position during total knee replacements.

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The device is designed to replace the standard plastic tibial trial spacer and uses proprietary technology to give surgeons real-time feedback on limb alignment and implant position.

OrthoSensor also announced recently that Stryker’s orthopedics division will co-market the VERASENSE.

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