CAPSURE EPICARDIAL PACING LEAD
FDA premarket approval P950024/S052 · decided 2013-10-17
Approval details
- PMA number
- P950024
- Supplement
- S052
- Supplement type
- 30-Day Notice
- Trade name
- CAPSURE EPICARDIAL PACING LEAD
- Generic name
- Permanent defibrillator electrodes
- Applicant
- Medtronic, Inc.
- Date received
- 2013-09-30
- Decision date
- 2013-10-17
- Days to decision
- 17 days
- Decision code
- OK30
- Product code
- NVY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- UPDATE TO THE MANUFACTURING AND INSPECTION PROCESS FOR TUBING USED IN MEDTRONIC CRDM THERAPY DELIVERY PRODUCTS.
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