Next-Generation SURGIMAP 2.0 SoftwareIn Corporate
FDA clears next-generation SURGIMAP 2.0 software, first pre-operative planning platform for personalized spinal implants. software tool allows surgeons to preoperatively select spinal implant size and plan patient-specific countoured spine rods with latest clinical data.
K-JAWS® : FDA approval in the USIn Corporate
MEDICREA has just obtained FDA approval to market its K-JAWS® Cervical Compression Staple in the United States “Given this technology’s highly innovative aspect and its unique design on the market, this approval process was the longest and most complex we have every had to administer with the FDA, but we have now reached a decisive milestone,” says Denys SOURNAC, Chairman and CEO of MEDICREA.