Tyber Medical Receives FDA 510(k) Clearance of BioTy-treated Headless Screw

Tyber Medical received FDA 510(k) clearance of BioTy™ Modified Surface Treatment for use on its Headless Screw System. Further, the company expanded its exclusive licensing agreement with Northeastern University to further enhance BioTy proprietary technology and IP.

BioTy nano-scale technology is designed to modify the surface...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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