# Medtronic Heart Valves

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 4 (1979–2006): 3 510(k) clearances and 1 original PMA approval
- Product codes: KRH (3), LWR (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 5 (1 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
- The Heart Valve Div. Medtronic Cardiovascular Surg: 1 (https://510kreport.com/company/heart-valve-div-medtronic-cardiovascular-surg)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Firms that cite its devices most
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Micardia Corporation: 1 (https://510kreport.com/company/micardia)
- Sciencity Co., Ltd.: 1 (https://510kreport.com/company/sciencity)

## Its most-cited devices
- K032810: Duran Band (Model H607H), Duran Ring (Model 610R), Duran Band (Model 610B), Duran Ancore Ring (Model 620R), Duran Ancore (2003), cited by 2
- K052860: CG Future Annuloplasty Band (2005), cited by 2
- K052970: Simplici-T Annuloplasty System (2006), cited by 1

## Recent decisions
- K052970: Simplici-T Annuloplasty System (Jan 11, 2006)
- K052860: CG Future Annuloplasty Band (Nov 10, 2005)
- K032810: Duran Band (Model H607H), Duran Ring (Model 610R), Duran Band (Model 610B), Duran Ancore Ring (Model 620R), Duran Ancore (Dec 5, 2003)
- P790007: Hancock Modified Orifice Bioprosthesis (Nov 15, 1979)

Source page: https://510kreport.com/company/medtronic-heart-valves