> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Anika Gains Rotator Cuff Implant Clearance
- URL: https://www.fdaweb.com/anika-gains-rotator-cuff-implant-clearance/
- Published: 2023-08-18T12:00:00.000Z
- Updated: 2026-09-14T18:51:34.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5155132

FDA has cleared an Anika Therapeutics 510(k) for the Integrity Implant System, intended for use in augmenting an injured tendon to promote healing in rotator cuff repair procedures. “Clearance of the hyaluronic acid (HA) based patch component joins the prior 510(k)s received for the associated fixation devices and instrumentation,” the company says. The implant provides an HA-based scaffold to provide improved strength and regenerative capacity over first-generation collagen patches, and supports regenerative healing through improved cell infiltration, tissue remodeling, and tendon thickening, it says.