VARIOUS FAMILIES OF ICD'S
FDA premarket approval P980016/S103 · decided 2007-06-29
Approval details
- PMA number
- P980016
- Supplement
- S103
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VARIOUS FAMILIES OF ICD'S
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2007-05-31
- Decision date
- 2007-06-29
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- CHANGE IN VENDOR FOR THE 11V AND 22V ZENER DIODES USED IN THE HYBRID OF IMPLANTABLE CARDIOVERTER DEFIBRILLATORS AND CARDIAC RESYNCHRONIZATION THERAPY DEVICES.
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