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# FDA Clears Zimmer Biomet Shoulder System
- URL: https://www.fdaweb.com/fda-clears-zimmer-biomet-shoulder-system/
- Published: 2018-01-03T12:00:00.000Z
- Updated: 2026-09-14T23:10:40.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5140408

FDA has cleared a Zimmer Biomet Holdings 510(k) for the Sidus Stem-Free Shoulder system as a total shoulder arthroplasty solution for patients with good bone stock who have either osteoarthritis, post-traumatic arthrosis, focal avascular necrosis of the humeral head or who had previous surgeries of the shoulder that do not compromise the fixation. The device is designed to anatomically restore a patient’s anatomy, preserve bone stock and allow for improved pre to post-operative patient outcomes, according to the company. It also contributes to reduced pain and restored range of motion, it says.