# K971617: Endoscopic Ventricular Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Integra Neurocare, LLC
- Decided: Jul 31, 1997 after 90 days
- Product code: JXG (Shunt, Central Nervous System And Components)
- Device class: 2
- Regulation: 21 CFR 882.5550
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K153041: Bundled Neurological Shunts and Accessories Product Families Labeling Modification to Support MR Conditional Labeling (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K971617
Methodology: https://510kreport.com/methodology