OVATIO CRT & SITUS OTW LV
FDA premarket approval P060027/S009 · decided 2009-03-04
Approval details
- PMA number
- P060027
- Supplement
- S009
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Postapproval Study Protocol - OSB
- Trade name
- OVATIO CRT & SITUS OTW LV
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2008-12-17
- Decision date
- 2009-03-04
- Days to decision
- 77 days
- Decision code
- APPR
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.
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