Curiteva earns FDA nod for spinal instrument system

Spinal Tech

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. 

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