# K241244: CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cerenovus, Inc.
- Decided: Oct 16, 2024 after 167 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: 10 generations back to K003880 (2001). 15 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K202752: AXS Vecta 46 Intermediate Catheter, Stryker Neurovascular (2021) Summary page 5.

## Most influential descendants
- K262398: CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set (2026), 0 descendants of its own

## Indications for use
The CEREGLIDE 42 Intermediate Catheter and the CEREGLIDE 57 Intermediate Catheter are indicated for use in facilitating the insertion and guidance of appropriately sized interventional devices into a selected blood vessel in the neurovascular system. The CEREGLIDE 57 Intermediate Catheter is also indicated for use as a conduit for retrieval devices.

Source page: https://510kreport.com/device/K241244
Methodology: https://510kreport.com/methodology