IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (ICD) GEM
FDA premarket approval P900061/S065 · decided 2006-11-07
Approval details
- PMA number
- P900061
- Supplement
- S065
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (ICD) GEM
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2006-05-10
- Decision date
- 2006-11-07
- Days to decision
- 181 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- APPROVAL FOR THE ADDITION OF A PAPERLESS CHART RECORDER TO THE STERILIZATION OPERATIONS.
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