Sprint Quattro, Subcutaneous Lead, Transvene CS/SVC Lead
FDA premarket approval P920015/S240 · decided 2020-01-10
Approval details
- PMA number
- P920015
- Supplement
- S240
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Sprint Quattro, Subcutaneous Lead, Transvene CS/SVC Lead
- Generic name
- Permanent defibrillator electrodes
- Applicant
- Medtronic, Inc.
- Date received
- 2019-12-17
- Decision date
- 2020-01-10
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- NVY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Add new inspections of the Packaging Tray assembly process for SelectSecure, Transvene CS/SVC and Sprint Quattro leads.
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510(k) clearances by this applicant
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