# K243180: SSPC NXT Delivery Catheter

- Pathway: 510(k) (Special)
- Applicant: CenterPoint Systems, LLC
- Decided: Dec 4, 2024 after 65 days
- Product code: DQY (Catheter, Percutaneous)
- 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K081931: SSPC Delivery Catheter. Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Most influential descendants
- K262240: SSPC NXT Delivery Catheter (2026), 0 descendants of its own

## Indications for use
The Delivery Catheter is intended for the venous introduction of pacing or defibrillation leads.

Source page: https://510kreport.com/device/K243180
Methodology: https://510kreport.com/methodology