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The algorithm correctly detected tumors in 26 cores in the validation study that were originally reported as tumor negative, the company said. Read More
GE Healthcare and Medtronic have gained FDA 510(k) clearance and the EU CE mark for an integration of two Medtronic technologies with GE Healthcare's CARESCAPE monitors that will allow physicians to continuously monitor patients at the bedside and in transport as well as automatically transmit data to their electronic medical records. Read More
In a clinical trial, the device successfully achieved fast, reliable biomechanical closure and rapidly stopped the flow of blood, the company said. Read More
The gentamicin-eluting ceramic bone void filler is intended for use in skeletally mature patients as an adjunct to systemic antibiotic therapy and surgical debridement. Read More
The system combines image-based procedure planning and real-time monitoring with hands-free precise robotic insertion and nonlinear steering. Read More