# The Heart Valve Div. Medtronic Cardiovascular Surg

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 5 (1991–1998): 5 510(k) clearances
- Product codes: KRH (3), LDF (2)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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 Blood Systems, Inc.: 1 (https://510kreport.com/company/medtronic-blood-systems)

## Firms that cite its devices most
- Medtronic Heart Valves: 1 (https://510kreport.com/company/medtronic-heart-valves)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Its most-cited devices
- K980534: Duran Flexible Annuloplasty Ring Model Number H608H (1998), cited by 1
- K960356: Posterior Annuloplasty Band (Model 607) (1996), cited by 1

## Recent decisions
- K980534: Duran Flexible Annuloplasty Ring Model Number H608H (Apr 30, 1998)
- K960356: Posterior Annuloplasty Band (Model 607) (Aug 27, 1996)
- K944956: Unipolar Pediatric Temporary Pacing Lead, Model 6491 (Jul 14, 1995)
- K922269: Unipolar Temporary Myocardial Pacing Wire, 6493 (Nov 23, 1992)
- K914602: Duran Flex Annuloplasty Ring/Obtur H601H, Modified (Nov 22, 1991)

Source page: https://510kreport.com/company/heart-valve-div-medtronic-cardiovascular-surg