# K133224: Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded W/ #2 Hifi Sutures

- Pathway: 510(k) (Special)
- Applicant: Conmed Corporation
- Decided: Jan 3, 2014 after 74 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: 11 generations back to K911837 (1991). 80 ancestors in all.
12 later devices descend from it; 6 cite it directly.
0 of 93 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131035: Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MM, Linvatec Corporation D/B/A Conmed Linvatec (2013) Summary page 1.

## Most influential descendants
- K192709: Fixone All Suture Anchor (2020), 3 descendants of its own
- K233429: OTS 25 (100-1) (2023), 2 descendants of its own
- K241234: OTS 25-L (100-5) (2025), 1 descendant of its own
- K202663: Suture Wing (2021), 1 descendant of its own
- K171465: Stryker Self-Punching ICONIX (2017), 1 descendant of its own

## Indications for use
The non-absorbable suture anchors are intended to reattach soft tissue to bone in orthopedic surgical procedures. The Y-Knot All-Suture Anchors may be used in either arthroscopic or open surgical procedures. After the suture strands are anchored to the bone, they may be used to reattach soft tissue, such as ligaments, tendons, or joint capsules to the bone. In conjunction with appropriate postoperative immobilization throughout the healing period, the suture anchor systems stabilize the damaged soft tissue.

Source page: https://510kreport.com/device/K133224
Methodology: https://510kreport.com/methodology