# Medtronic Cardiac Rhythm Disease Management

- Location (FDA's records): Mounds View
- FDA decisions: 8 (1979–2005): 8 original PMA approvals
- Product codes: NVN (3), LWP (2), LWS (2), NIK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 23 (4 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- P030036: Medtronic Selectsecure Lead Model 3830 (Aug 3, 2005)
- P010031: Concerto/Insync Sentry/Insync Maximo Implantable Cardiovascular Defibrillators with Cardiac Resynchicnization (Jun 26, 2002)
- P980016: Virtuso/Entrust/Maximo/Intrinsic/Marquis/Implantable Cardiverter Defibrillators (Oct 9, 1998)
- P900061: Medtronic PCD Tachyarrhythmia Control System (Feb 11, 1993)
- P830061: Steroid Tip (TM) Model 4503&4003 Transvenous Pacing (Jul 29, 1986)
- P850089: Capsure SP, Capsure, Capsure 2 Leads, Excellence S, Impulse, Impluse II Excellence SS, Leads (Jul 29, 1986)
- P820003: Versatrax Model 7000 Universal a-V Pulse Generator (Nov 16, 1982)
- P780009: Byrel Programable Pacemaker (Mar 27, 1979)

Source page: https://510kreport.com/company/medtronic-cardiac-rhythm-disease-management