# K012617: Jostra Arterial Perfusion Cannulae, Model a...

- Pathway: 510(k) (Traditional)
- Applicant: Jostra AG
- Decided: Nov 6, 2001 after 85 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 Pediatric Arterial Cannulae: named in the summary without a submission number

## Most influential descendants
- K023251: Pediatric Arterial Cannula (2002), 0 descendants of its own

## Indications for use
The Jostra Pediatric Arterial Cannulae are designed to be used as perfusion cannulae to return arterial blood from the extracoproeal circuit to the patient during cardiopulmonary bypass up to 6 hours or less.

Source page: https://510kreport.com/device/K012617
Methodology: https://510kreport.com/methodology