Platinium VR and Platinium DR ICDs
FDA premarket approval P980049/S138 · decided 2020-08-10
Approval details
- PMA number
- P980049
- Supplement
- S138
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Platinium VR and Platinium DR ICDs
- Generic name
- DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2020-07-13
- Decision date
- 2020-08-10
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MRM
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- Introduction of automated equipment during the manufacturing of select pacemakers and defibrillators.
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