# K122374: Arthrex Suture (Uhmwpe)

- Pathway: 510(k) (Special)
- Applicant: Arthrex, Inc.
- Decided: Sep 25, 2012 after 50 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K904436 (1990). 31 ancestors in all.
13 later devices descend from it; 10 cite it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041553: Arthrex Suture Grafting Kit, Arthrex, Inc. (2004) Summary page 1.
- K100652: Acl Tightrope, Arthrex, Inc. (2010) Summary page 1.

## Most influential descendants
- K171296: SutureTape (2017), 3 descendants of its own
- K152868: ExpressBraid Graft Manipulation (2016), 2 descendants of its own
- K193575: Arthrex SutureTape (2020), 1 descendant of its own
- K253910: Stitch - Suture Wires and Tapes (2026), 0 descendants of its own
- K260018: Arthrex FiberButton (2026), 0 descendants of its own

## Indications for use
The Arthrex Suture is intended for use in soft tissue approximation and/or ligation. The suture may be provided individually or be incorporated as a component, into surgeries where constructs including those with allograft or autograft tissue are used for repair.

Source page: https://510kreport.com/device/K122374
Methodology: https://510kreport.com/methodology