K2M receives FDA 510(k) clearance for the MESA 2 Deformity Spinal System

According to a news report, K2M has received FDA clearance for its new MESA 2 Deformity Spinal System.

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K2M’s President and CEO Eric Major noted in the report, “FDA clearance of MESA 2 is a milestone event for K2M that further enhances our position in the global spine surgery market.” The MESA 2 is the next generation of the company’s established MESA spinal device.

To learn more about K2M and their wide variety of medical devices, click here.

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