Cardiac Resynchronization Therapy Defibrillator
FDA premarket approval P060027/S099 · decided 2019-03-05
Approval details
- PMA number
- P060027
- Supplement
- S099
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Cardiac Resynchronization Therapy Defibrillator
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2019-02-05
- Decision date
- 2019-03-05
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- Addition of a pre-conditioning step prior to the Electrical Wafer Sorting test.
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