# K244025: Argo Knotless GENESYS Anchor

- Pathway: 510(k) (Special)
- Applicant: Conmed Corporation
- Decided: Jan 28, 2025 after 32 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: 12 generations back to K911837 (1991). 72 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 74 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240090: Argo Knotless GENESYS Anchor, Conmed Corporation (2024) Summary page 5.

## Most influential descendants
- K252946: BioBrace® Extra-Articular Ligament Augmentation Kit (2025), 0 descendants of its own

## Indications for use
The biocomposite suture anchor is intended to reattach soft tissue to bone in orthopedic surgical procedures. The Argo Knotless® GENESYS™ Anchor may be used in either arthroscopic or open surgical procedures. After the suture is anchored to the bone, it may be used to reattach soft tissue, such as ligaments, tendons, or joint capsules to the bone. The suture anchor system thereby stabilizes the damaged soft tissue, in conjunction with appropriate postoperative immobilization throughout the healing period.

Source page: https://510kreport.com/device/K244025
Methodology: https://510kreport.com/methodology