MEDTRONIC MODEL 7250 ARRHYTHMIA MANAGEMENT DEVICE
FDA premarket approval P980050/S007 · decided 2001-08-08
Approval details
- PMA number
- P980050
- Supplement
- S007
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MEDTRONIC MODEL 7250 ARRHYTHMIA MANAGEMENT DEVICE
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic, Inc.
- Date received
- 2001-07-17
- Decision date
- 2001-08-08
- Days to decision
- 22 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- CHANGE IN THE SUPPLIER OF POLYETHERURETHANE.
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