CONCERTO II CRT-D, CONSULTA CRT-D, MAXIMO II CRT-D, PROCTECTA CRT-D,PROTECTA XT CRT-D
FDA premarket approval P010031/S460 · decided 2014-08-27
Approval details
- PMA number
- P010031
- Supplement
- S460
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- CONCERTO II CRT-D, CONSULTA CRT-D, MAXIMO II CRT-D, PROCTECTA CRT-D,PROTECTA XT CRT-D
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2014-08-05
- Decision date
- 2014-08-27
- Days to decision
- 22 days
- Decision code
- OK30
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- AUTOMATE THE IN-PROCESS BATTERY INSULATOR INSPECTION.
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