# K060959: Symmetry Balloon Dilatation Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corporation
- Decided: Apr 12, 2006 after 5 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
Longest line of descent: 1 generation back to K953602 (1995). 2 ancestors in all.
1 later device descends from it; 1 cites 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)
- K953602: Symmetry Small Vessel Balloon Dilatation Catheter, Boston Scientific Corp (1995) Summary page 1.
- K000798: Talon Balloon Dilation Catheter, Boston Scientific Corp (2000) Summary page 2.

## Most influential descendants
- K143193: Symmetry and Symmetry Stiff Shaft Balloon Dilatation Catheters (2015), 0 descendants of its own

## Indications for use
Symmetry and Symmetry Stiff Shaft Balloon Dilatation Catheters are recommended for Percutaneous Transluminal Angioplasty of small, narrowed or obstructed iliac, femoral, or renal vessels in the peripheral vasculature.

Source page: https://510kreport.com/device/K060959
Methodology: https://510kreport.com/methodology