CADENCE TIERED-THERAPY DEFIBRILLATOR SYSTEM
FDA premarket approval P910023/S142 · decided 2007-07-10
Approval details
- PMA number
- P910023
- Supplement
- S142
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- CADENCE TIERED-THERAPY DEFIBRILLATOR SYSTEM
- Generic name
- Pulse generator, permanent, implantable
- Applicant
- ABBOTT MEDICAL
- Date received
- 2007-05-21
- Decision date
- 2007-07-10
- Days to decision
- 50 days
- Decision code
- APPR
- Product code
- NVZ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- APPROVAL FOR SOFTWARE MODIFICATIONS TO THE HOUSECALL PLUS SYSTEM SOFTWARE (RECEIVER SOFTWARE MODEL 4000 VERSION 3.1) WHICH MERGES THE HOUSECALL RECEIVER 3.0.3 AND THE MATRIX PCS 2.0 SOFTWARE VERSION.
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