Curiteva Gains 510(k) for Inspire 3D Porous PEEK HAFuse Cervical Interbody

Curiteva Inspire Porous PEEK Cervical Interbody System

Curiteva announces what it states is the first FDA 510(k)-cleared 3D-printed PEEK implant, the Inspire Porous PEEK Cervical Interbody System with HAFUSE Technology. The company plans a commercial launch in key academic centers across the United States.

The Inspire platform is manufactured with a proprietary, patented Fused Filament Fabrication...

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JV

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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