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# Medicrea 510(k) Cleared for 3D-Printed Spinal Cage
- URL: https://www.fdaweb.com/medicrea-510-k-cleared-for-3d-printed-spinal-cage/
- Published: 2018-06-01T12:00:00.000Z
- Updated: 2026-09-15T00:09:55.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141579

FDA has cleared a Medicrea Group 510(k) for patient-specific spinal cages through the extension of its UNiD ASI (Adaptive Spine Intelligence) technology to select from its IB3D range of 3D-printed titanium interbody devices. The clearance allows Medicrea to digitally plan, manufacture in-house and supply a 3D-printed device that has been “optimized to follow each patient’s unique spinal anatomy using the company’s proprietary \[artificial intelligence\]-driven UNiD technology,” Medicrea says.