# K201786: Arthrex Mini Hip PushLock

- Pathway: 510(k) (Special)
- Applicant: Arthrex, Inc.
- Decided: Jul 30, 2020 after 30 days
- Product code: MAI (Fastener, Fixation, Biodegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K961555 (1996). 13 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151092: Arthrex Short Suture Anchors, Arthrex, Inc. (2016) Summary page 4.

## Most influential descendants
- K253931: Arthrex Bioabsorbable PushLock Suture Anchors (2026), 1 descendant of its own
- K212381: VersaTap, VersaLat, DueLock, VersaTi, MiniTi (2021), 1 descendant of its own
- K262357: Arthrex Bioabsorbable PushLock Suture Anchors (2026), 0 descendants of its own
- K250544: Knotilus+ Biocomposite Knotless Anchor (2025), 0 descendants of its own
- K242296: VersaTap™ Suture Anchor (ADP050); VersaPEEK™ Suture Anchor (APP002); MicroTi™ Suture Anchor (ATP003-M); VersaLat™ Ti Suture Anchor (ADP021-TI); VersaLat™ Suture Anchor (ADP021-PK) (2024), 0 descendants of its own

## Indications for use
The Arthrex Mini Hip PushLock is intended to be used for suture (soft tissue) to bone in the hip. Specifically, Acetabular Labral Repair.

Source page: https://510kreport.com/device/K201786
Methodology: https://510kreport.com/methodology