# K000776: Medtronic DLP Arterial Cannulae with 3D Tip

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Cardiac Surgical Products
- Decided: Feb 7, 2001 after 334 days
- Product code: DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4210
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
13 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K013013: Medtronic DLP Arterial Cannula with 3D Tip - 22 FR. (2001), 12 descendants of its own
- K033416: Select 3D Arterial Cannula with Carmeda Bioactive Surface and Select Cap Arterial Cannula with Carmeda Bioactive Surface (2003), 11 descendants of its own
- K043179: Select 3D Arterial Cannula (2005), 10 descendants of its own
- K061254: Eopa 3D Arterial Cannula, Models 78220,78222,78320,783222 (2006), 8 descendants of its own
- K111972: Affinity CP Centrifugal Pump, Resting Heart Sys.,Myotherm Cardioplegia Deliv.,Affinity Hollow Fiber Oxygenator,Aaf (2011), 5 descendants of its own

## Recalls of this device
- Jan 30, 2014 · Class II · Z-0997-2014: Medtronic is recalling all models of its Select 3D and Select CAP Arterial Cannula product families due to reports of the cannula body splitting near the suture collar.

Source page: https://510kreport.com/device/K000776
Methodology: https://510kreport.com/methodology