VIRTUSO/ENTRUST/MAXIMO/INTRINSIC/MARQUIS/IMPLANTABLE CARDIVERTER DEFIBRILLATORS
FDA premarket approval P980016/S571 · decided 2016-03-08
Approval details
- PMA number
- P980016
- Supplement
- S571
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VIRTUSO/ENTRUST/MAXIMO/INTRINSIC/MARQUIS/IMPLANTABLE CARDIVERTER DEFIBRILLATORS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2016-02-08
- Decision date
- 2016-03-08
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Implementation of the following previously accepted manufacturing changes: 1) the removal of various visual inspections and re-ordering of steps in final packaging; 2) a change to the high voltage capacitor weld monitoring frequency; and 3) an update to the manufacturing execution system to FACTORYworks 9.1 and associated changes.
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