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# FDA Clears Zimmer Nexel Elbow System
- URL: https://www.fdaweb.com/fda-clears-zimmer-nexel-elbow-system/
- Published: 2016-03-03T12:00:00.000Z
- Updated: 2026-09-15T02:40:39.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5134957

> FDA has cleared a Zimmer Biomet Holdings 510(k) for the compatibility of the Nexel Total Elbow System with the Comprehensive Segmental Revision System (SRS). The distal component of the SRS humeral system when combined with Nexel is designed for elbow replacement, while the remaining components allow for proximal or total humeral reconstruction when used with the glenoid component of the Comprehensive Shoulder System, according to the company. “In addition to addressing proximal, distal or complete humeral replacement, the ability of the Comprehensive SRS and Nexel Total Elbow to interact with the Regenerex Tissue Attachment Augments addresses concerns regarding graft availability and resorption as well as providing tissue stabilization and attachment points,” the company says.