# K020515: Jostra Antegrade Cardioplegia Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Jostra AG
- Decided: Apr 24, 2002 after 68 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- 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. The FDA summary names its predicate without a number.
- (no number) Medtronic DLP Antegrade Cardioplegia Cannula: named in the summary without a submission number

## Most influential descendants
- K140569: Antegrade Cardioplegia Cannula (N-Type) (2014), 0 descendants of its own

## Indications for use
The Jostra Antegrade Cardioplegia Cannulas are intended to be used to infuse blood and/or cardioplegia solution to the patient's myocardium, antegrade, via the aortic, root, during cardiopulmonary bypass for 6 hours or less.

Source page: https://510kreport.com/device/K020515
Methodology: https://510kreport.com/methodology