PARADYM CRT-D 8750,PARADYM RF CRT-D 9750 (ZL101), PARADYM RF CRT-D 9750 (ZL 102) AND INTENSIA CRT-D
FDA premarket approval P060027/S075 · decided 2015-03-19
Approval details
- PMA number
- P060027
- Supplement
- S075
- Supplement type
- 30-Day Notice
- Trade name
- PARADYM CRT-D 8750,PARADYM RF CRT-D 9750 (ZL101), PARADYM RF CRT-D 9750 (ZL 102) AND INTENSIA CRT-D
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2015-02-24
- Decision date
- 2015-03-19
- Days to decision
- 23 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- ADD AN ALTERNATE SUPPLIER FOR THE GLUE USED IN THE DIE ATTACH PROCESS FOR THE HYBRIDS USED IN THE DEVICES.
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