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# Globus Knee Arthroplasty Cleared for ExcelsiusFlex
- URL: https://www.fdaweb.com/globus-knee-arthroplasty-cleared-for-excelsiusflex/
- Published: 2024-07-18T12:00:00.000Z
- Updated: 2026-09-14T14:35:52.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157382

FDA has cleared a Globus Medical 510(k) for its ExcelsiusFlex with total knee arthroplasty option. The new robotic navigation platform is designed to offer surgeons control, resection accuracy, and procedural flexibility in total knee arthroplasty, according to the company. Additionally, it says Actify 3D Total Knee System for use on the ExcelsiusFlex platform received a 510(k) clearance.

ExcelsiusFlex is “engineered to assist the surgeon in primary total knee arthroplasty procedures for robotically guided resections based on their implant placement planning,” Globus says. Actify 3D is designed to pair cementless reconstruction with operative efficiency and anatomic fit, it says. “Whether through manual or robotic-assisted workflows, Actify 3D is additive-engineered to combine strength and a porous lattice interface conducive to cementless fixation,” it adds.