Huntsville, AL based mostly know-how firm Curiteva® proclaims FDA 510(ok) clearance to market a Navigation Instrument System to enhance their Prodigy® Pedicle Screw System and SI-LUTION® Sacroiliac Joint Fusion Programs. The pioneers in 3D printed PEEK interbody fusion know-how designed these devices to combine seamlessly with the market main navigation system helping surgeons in exactly finding anatomical constructions for open and MIS procedures. The system contains reusable awls, probes, faucets, drills, and drivers and is avaiable for business launch.
“Only a few corporations have been in a position to mix a extremely engineered implant with user-friendly instrumentation. Curiteva’s SI-LUTION does simply that and extra. Now the SI-LUTION system affords surgeons the arrogance and reliability of utilizing navigation,” said Dr. Troy Morrison, CMH Orthopedic and Backbone Middle.
“We’re effectively positioned with world-class scalable manufacturing to develop devices to additional leverage a surgeons’ capability to validate implant placement, whereas lowering total radiation publicity and OR time. This thrilling addition to our portfolio builds on the Curiteva dedication to ship secure, revolutionary, and efficient merchandise to our prospects .” commented Government Vice President, Mark Mohlman.
Curiteva is a privately held know-how and manufacturing firm devoted to advancing spine surgical procedure and enhancing medical outcomes by partnering with suppliers and suppliers to ship revolutionary and intuitive implant programs to the market. Our enterprise is based on a dedication to constructing world-class manufacturing, accelerating analysis and growth, sustaining lean operational self-discipline, and delivering novel know-how to fulfill the evolving wants of our prospects and the sufferers they serve. For extra data, please go to www.curiteva.com.