# K163259: AXS Offset Delivery Assist Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Neurovascular
- Decided: Jul 28, 2017 after 249 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K172014: Wedge Microcatheter (2018), 3 descendants of its own
- K230609: NG Delivery Catheter (2023), 1 descendant of its own
- K252569: Carrier XL Delivery Catheter (2025), 0 descendants of its own
- K232542: Wedge XL Delivery Catheter (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K163259
Methodology: https://510kreport.com/methodology