# K241637: Echo Intracranial Base Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Neurovascular
- Decided: Dec 19, 2024 after 195 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- 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
Longest line of descent: 9 generations back to K010954 (2001). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193034: AXS Infinity LS Plus Long Sheath, Stryker Neurovascular (2019) Summary page 6.

## Indications for use
The Echo Intracranial Base Catheter is indicated for the introduction of interventional devices into the neurovasculature.

Source page: https://510kreport.com/device/K241637
Methodology: https://510kreport.com/methodology