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# FDA Clears DJO Global Hip Revision Device
- URL: https://www.fdaweb.com/fda-clears-djo-global-hip-revision-device/
- Published: 2017-03-16T12:00:00.000Z
- Updated: 2026-09-14T22:12:10.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5138222

FDA has cleared a DJO Global 510(k) for its Exprt Revision Hip. “The two-tray revision system represents an 80-90% reduction in instruments compared to competitive systems,” the company says. The device features 3 degree taper geometry for axial stability, and “optimized splines providing 0.2mm of press-fit on each side of the conical region,” DJO adds. It comes in total construct lengths from 195-295mm, and an anatomic anterior distal relief curved in multiple planes.