# K252144: Iconix Speed Anchor; Iconix Speed HA+ Anchor

- Pathway: 510(k) (Special)
- Applicant: Riverpoint Medical
- Decided: Jul 30, 2025 after 22 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 13 generations back to K961555 (1996). 33 ancestors in all.
No later device cites it as a predicate yet.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233468: Iconix Anchor, Riverpoint Medical (2023) Summary page 5.

## Indications for use
Iconix Speed Anchors are intended to be used for soft-tissue to bone fixation in the shoulder. They are indicated for use in rotator cuff repair.

Source page: https://510kreport.com/device/K252144
Methodology: https://510kreport.com/methodology