Open Pivot Heart Valve
FDA premarket approval P990046/S051 · decided 2017-10-06
Approval details
- PMA number
- P990046
- Supplement
- S051
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Open Pivot Heart Valve
- Generic name
- HEART-VALVE, MECHANICAL
- Applicant
- Medtronic Ats Medical, Inc.
- Date received
- 2017-09-07
- Decision date
- 2017-10-06
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LWQ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Transfer of sewing operations for several Open Pivot Heart Valve models to Medtronic Tijuana, Mexico.
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