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# Guide on Bone Anchor 510(k)s
- URL: https://www.fdaweb.com/guide-on-bone-anchor-510-k-s/
- Published: 2020-03-03T12:00:00.000Z
- Updated: 2026-09-14T16:05:31.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146225

*Federal Register* notice: FDA has made available a final guidance entitled “Bone Anchors — Premarket Notification (510(k)) Submissions.” The document provides recommendations for 510(k) submissions for bone anchor (suture anchor) devices, including performance testing recommendations and device descriptions. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-03-03/pdf/2020-04361.pdf?ref=fdaweb.com).