Platinium CRT-D 1711; Platinium CRT-D 1741
FDA premarket approval P060027/S082 · decided 2016-08-08
Approval details
- PMA number
- P060027
- Supplement
- S082
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Platinium CRT-D 1711; Platinium CRT-D 1741
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2016-07-14
- Decision date
- 2016-08-08
- Days to decision
- 25 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- Use of the Automated Optical Inspection equipment during the microelectronic and electronic assembly manufacturing.
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