# K024178: Viatorr Endoprosthesis

- Pathway: 510(k) (Traditional)
- Applicant: W. L. Gore & Associates, Inc.
- Decided: Mar 7, 2003 after 79 days
- Product code: JCT (Prosthesis, Tracheal, Expandable)
- Device class: 2
- Regulation: 21 CFR 878.3720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) VIABAHN™ Endoprosthesis: named in the summary without a submission number
- (no number) Ultraflex™ Tracheobronchial Stent System: named in the summary without a submission number
- (no number) WALLGRAFT® Tracheobronchial Endoprosthesis with Unistep Plus Delivery System: named in the summary without a submission number

## Indications for use
The VIATORR® Endoprosthesis is indicated for the treatment of tracheobronchial strictures produced by malignant neoplasms.

Source page: https://510kreport.com/device/K024178
Methodology: https://510kreport.com/methodology