QuickFlex u, Quartet Cardiac Resynchronization Therapy (CRT) Passive Fixation Leads
FDA premarket approval P030054/S366 · decided 2018-12-05
Approval details
- PMA number
- P030054
- Supplement
- S366
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- QuickFlex u, Quartet Cardiac Resynchronization Therapy (CRT) Passive Fixation Leads
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- ABBOTT MEDICAL
- Date received
- 2018-11-23
- Decision date
- 2018-12-05
- Days to decision
- 12 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- Introduce periodic particulate matter testing and equipment to the Malaysia and Puerto Rico manufacturing facilities.
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