VIRTUOSO FAMILY OF DEVICES
FDA premarket approval P980016/S106 · decided 2007-09-12
Approval details
- PMA number
- P980016
- Supplement
- S106
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VIRTUOSO FAMILY OF DEVICES
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2007-08-13
- Decision date
- 2007-09-12
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- REWORK PROCESS FOR A COMPONENT DURING THE MANUFACTURING PROCESS.
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