CONCERTO ICD,CONCERTO II CRT-D,CONSULTA DF4 ICD,CONSULTA ICD,INSYNC III MARQUIS ICD,INSYNC MAXIMO ICD,BRAVA CRT-D,VIVA S
FDA premarket approval P010031/S370 · decided 2013-05-03
Approval details
- PMA number
- P010031
- Supplement
- S370
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- CONCERTO ICD,CONCERTO II CRT-D,CONSULTA DF4 ICD,CONSULTA ICD,INSYNC III MARQUIS ICD,INSYNC MAXIMO ICD,BRAVA CRT-D,VIVA S
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2013-04-08
- Decision date
- 2013-05-03
- Days to decision
- 25 days
- Decision code
- OK30
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- IMPLEMENTATION OF AN UPDATED ACCEPTANCE CRITERION FOR EVALUATION OF INSULATOR MATERIALS USED IN THE MANUFACTURE OF THE SUBJECT ICDS AND CRT-D DEVICES.
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