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# FDA Clears FX Shoulder 510(k) for Shoulder Prosthesis
- URL: https://www.fdaweb.com/fda-clears-fx-shoulder-510-k-for-shoulder-prosthesis/
- Published: 2021-02-19T12:00:00.000Z
- Updated: 2026-09-14T16:47:38.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148708

FDA has cleared an FX Shoulder 510(k) for the Easytech Stemless Anatomic, a shoulder prosthesis featuring primary peripheral fixation. The device’s design and Easytech Anchor base allows it to fit peripherally just inside the cortical bone where bone quality is optimal for fixation, the company says. It is intended to treat a severely painful or disabled shoulder joint, caused by osteoarthritis, with a functional rotator cuff, it says. The cementless Anchor base is available in diameters of 30 to 42mm.