CONCERTO/II/CONSULTA/INSYNC ICD/MARQUIS/MAXIMO/II MARQUIS/MAXIMO II/II PROTECT/III MARQUIS/SENTRY/CONEXUS ACTIVATOR
FDA premarket approval P010031/S210 · decided 2010-08-13
Approval details
- PMA number
- P010031
- Supplement
- S210
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- CONCERTO/II/CONSULTA/INSYNC ICD/MARQUIS/MAXIMO/II MARQUIS/MAXIMO II/II PROTECT/III MARQUIS/SENTRY/CONEXUS ACTIVATOR
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2010-07-15
- Decision date
- 2010-08-13
- Days to decision
- 29 days
- Decision code
- OK30
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- IMPLEMENTATION OF AN ELECTRONIC SYSTEM FOR INCOMING INSPECTION DATA.
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