# K251668: SurfRider 13 Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Kaneka Americas Holding, Inc.
- Decided: Jan 5, 2026 after 220 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: 7 generations back to K945904 (1995). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210230: Phenom Catheters, Micro Therapeutics Lnc. D/B/A Ev3 Neurovascular (2021) Summary page 5.

## Indications for use
The SurfRider 13 Microcatheter is intended for the introduction of interventional devices, such as embolic coils, or diagnostic agents into the neurovasculature.

Source page: https://510kreport.com/device/K251668
Methodology: https://510kreport.com/methodology