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Kuros Biosciences Gains FDA Clearance for Intervertebral Body Fusion Device

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Kuros Biosciences received FDA clearance to market the Kuros Transforaminal Lumbar Interbody Fusion cage. The device is to be used with KUR-113, the company's Fibrin-PTH product candidate for spinal fusion. Clinical trials of the system will now commence.

The cage is available in a range of sizes and cleared for use in the lumbar spine in combination with autograft and/or allograft.

Source: Kuros Biosciences