THINLINE II/ FINELINE II
FDA premarket approval P960004/S030 · decided 2006-01-19
Approval details
- PMA number
- P960004
- Supplement
- S030
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- THINLINE II/ FINELINE II
- Generic name
- Permanent defibrillator electrodes
- Applicant
- Boston Scientific
- Date received
- 2005-12-22
- Decision date
- 2006-01-19
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- NVY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- ADDITION OF SECOND SUPPLIER FOR THE TUBING USED AS THE MAIN BODY TUBING ON THE FINELINE II / THINLINE II FAMILY OF LEADS.
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