# K211349: Selebrek PTCA Balloon Dilatation Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Kossel Medtech (Suzhou) Co., Ltd.
- Decided: Jan 7, 2022 after 249 days
- Product code: LOX (Catheters, Transluminal Coronary Angioplasty, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.5100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K042537 (2004). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180921: Sapphire II PRO Balloon Dilatation Catheter, Orbusneich Medical Trading, Inc. (2018) Summary page 4.

## Indications for use
The Selebrek PTCA Balloon Dilatation Catheter is indicated for balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion

Source page: https://510kreport.com/device/K211349
Methodology: https://510kreport.com/methodology