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# Arthrosurface Toe Fixation Cleared by FDA
- URL: https://www.fdaweb.com/arthrosurface-toe-fixation-cleared-by-fda/
- Published: 2019-09-05T12:00:00.000Z
- Updated: 2026-09-15T01:47:50.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5144934

FDA has cleared an Arthrosurface 510(k) for its BOSS Toe Fixation System, which the company says is intended to improve stabilization in a first metatarsal that presents with a distal bone void and provides patients with a motion-preserving alternative to toe fusion. The device was designed to fill the current void of treatment options available for failed synthetic implants, it says. It was also designed for patients who want to avoid joint fusion and regain their motion and active lifestyles. The device is intended to be used in conjunction with Arthrosurface’s existing line of HemiCAP DF implants and ToeMotion Systems.