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# 510(k) for Shoulder Arthroplasty Cleared
- URL: https://www.fdaweb.com/510-k-for-shoulder-arthroplasty-cleared/
- Published: 2018-11-05T12:00:00.000Z
- Updated: 2026-09-15T00:42:26.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5142744

FDA has cleared a Shoulder Innovations 510(k) for the InSet Humeral Short Stem System for partial or total shoulder arthroplasty used in the treatment of degenerative, rheumatoid or traumatic arthritis in the shoulder. The system includes streamlined instrumentation and proprietary coating technology for implant fixation with bone preservation, the company says. “The combination of the InSet Humeral Stem and Shoulder Innovation’s unique InSet glenoid implant affords a surgically simple, bone sparing option for many types of humeral or glenoid deformities associated with arthritis,” it adds.