# K261889: Trevo Trak 21 Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Stryker Neurovascular
- Decided: Jul 1, 2026 after 26 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: 6 generations back to K003086 (2001). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211594: Trevo Trak 21 Microcatheter, Stryker Neurovascular (2021) Summary page 5.

## Indications for use
The Microcatheter is indicated to provide vascular access for selective placement of devices and/or fluids, such as contrast media, within the neurovasculature, including large intracranial vessels (e.g., internal carotid artery [ICA] and middle cerebral artery [MCA]), during diagnostic and/or therapeutic procedures.

Source page: https://510kreport.com/device/K261889
Methodology: https://510kreport.com/methodology