# K213314: CerusEndo Microcatheter (027)

- Pathway: 510(k) (Traditional)
- Applicant: Cerus Endovascular, Inc.
- Decided: Mar 15, 2022 after 162 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 K960806 (1996). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142449: Headway 27 Microcatheter, MicroVention, Inc. (2015) Summary page 4.

## Indications for use
The CerusEndo Microcatheter (027) is intended to deliver therapeutic devices within the neurovasculature.

Source page: https://510kreport.com/device/K213314
Methodology: https://510kreport.com/methodology