MEDTRONIC MODEL 7223CX MICRO JEWEL II(TM)
FDA premarket approval P900061/S024 · decided 1996-11-08
Approval details
- PMA number
- P900061
- Supplement
- S024
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- MEDTRONIC MODEL 7223CX MICRO JEWEL II(TM)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 1996-04-24
- Decision date
- 1996-11-08
- Days to decision
- 198 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- APPROVAL FOR MEDTRONIC MODEL 7218 B/C/D/E WITH THE MODEL 9896 SOFTWARE AND THE MEDTRONIC MODEL 7223 CX MICRO JEWELL II WITH MODEL 5705 ACTIVE CAN EMULATOR AND MODEL 9955 SOFTWARE
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