Curiteva received FDA 510(k) approval for its pedicle and sacroiliac joint navigation instruments, the medtech company said Aug. 8.
The instruments compliment Curiteva's Prodigy pedicle screw system and SI-Lution SI joint fusion systems, according to a news release. The system is available for commercial release and has reusable awls, probes, taps, drills and drivers.
"We are well positioned with world-class scalable manufacturing to develop instruments to further leverage a surgeon's ability to validate implant placement while reducing overall radiation exposure and OR time," Curiteva Executive Vice President Mark Mohlman said in the release.