# K000798: Talon Balloon Dilation Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Jun 8, 2000 after 87 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K060959: Symmetry Balloon Dilatation Catheter (2006), 1 descendant of its own
- K143193: Symmetry and Symmetry Stiff Shaft Balloon Dilatation Catheters (2015), 0 descendants of its own
- K060960: Boston Scientific Talon Balloon Dilatation Catheter (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K000798
Methodology: https://510kreport.com/methodology