FINELINE II Lead Family
FDA premarket approval P960004/S082 · decided 2018-02-08
Approval details
- PMA number
- P960004
- Supplement
- S082
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- FINELINE II Lead Family
- Generic name
- Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
- Applicant
- Boston Scientific
- Date received
- 2018-01-11
- Decision date
- 2018-02-08
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- NVN
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Implementation of serial number reading stations with optical character recognition equipment and software for use in lead manufacturing.
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