# Medtronic Cardiac Surgery

- Location (FDA's records): Minneapolis
- FDA decisions: 2 (1981–2024): 1 510(k) clearance and 1 original PMA approval
- Product codes: LWQ (1), DTN (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Recent decisions
- K241053: MVR™ Venous Reservoir Bag 800 mL; MVR™ Venous Reservoir Bag 1600 mL; MVR™ Venous Reservoir Bag with Cortiva™  BioActive Surface 800 mL; MVR™ Venous Reservoir Bag with Cortiva™  BioActive Surface 1600 mL (May 15, 2024)
- P790018: Medtronic (R) Hall Prosthetic Heart Valve (Dec 23, 1981)

Source page: https://510kreport.com/company/medtronic-cardiac-surgery