JEWEL AF MODEL 7250
FDA premarket approval P980050/S071 · decided 2012-03-23
Approval details
- PMA number
- P980050
- Supplement
- S071
- Supplement type
- 30-Day Notice
- Trade name
- JEWEL AF MODEL 7250
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic, Inc.
- Date received
- 2012-02-29
- Decision date
- 2012-03-23
- Days to decision
- 23 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- UPDATES TO THE SOFTWARE USED TO DIRECT AND TRACK MANUFACTURING ACTIVITIES.
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