CTL Medical received FDA 510(k) clearance to market the MATISSE™ Titanium Anterior Cervical Interbody Fusion cage for use with supplemental fixation, such as the company’s VAN GOGH™ anterior cervical plate.
MATISSE features CTL’s proprietary TiCro™ surface technology, which is designed to offer 200% greater endplate contact surface area. The first version of MATISSE received its clearance in 2012 under AccelSPINE, which was acquired by CTL in 1Q16.
Sources: CTL Medical Corporation; ORTHOWORLD Inc.
CTL Medical received FDA 510(k) clearance to market the MATISSE™ Titanium Anterior Cervical Interbody Fusion cage for use with supplemental fixation, such as the company's VAN GOGH™ anterior cervical plate.
MATISSE features CTL's proprietary TiCro™ surface technology, which is designed to offer 200% greater endplate contact...
CTL Medical received FDA 510(k) clearance to market the MATISSE™ Titanium Anterior Cervical Interbody Fusion cage for use with supplemental fixation, such as the company’s VAN GOGH™ anterior cervical plate.
MATISSE features CTL’s proprietary TiCro™ surface technology, which is designed to offer 200% greater endplate contact surface area. The first version of MATISSE received its clearance in 2012 under AccelSPINE, which was acquired by CTL in 1Q16.
Sources: CTL Medical Corporation; ORTHOWORLD Inc.
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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.





