# K034058: Spherical Tip Coronary Ostial Cannula, Model 30011

- Pathway: 510(k) (Special)
- Applicant: Medtronic Vascular
- Decided: Jan 29, 2004 after 30 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
Longest line of descent: 1 generation back to K821149 (1982). 1 ancestor in all.
4 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K821149: Submission Coronary Cannula, Dlp, Inc. (1982) Summary page 1.

## Most influential descendants
- K131269: DLP Coronary Ostial Perfusion Cannulae (2013), 3 descendants of its own
- K141951: DLP Silicone Coronary Artery Ostial Cannulae (2014), 2 descendants of its own
- K231206: DLP Silicone Coronary Artery Ostial Cannulae (2023), 0 descendants of its own
- K230960: DLP™ Silicone Coronary Artery Ostial Cannulae (2023), 0 descendants of its own

## Indications for use
The Spherical Tip Coronary Ostial Cannula is intended for use in conjunction with cardiopulmonary bypass surgery up to six hours or less, for delivery of cardioplegia solutions directly to the coronary arteries.

Source page: https://510kreport.com/device/K034058
Methodology: https://510kreport.com/methodology