MYNX VASCULAR CLOSURE DEVICE
FDA premarket approval P040044/S029 · decided 2010-04-28
Approval details
- PMA number
- P040044
- Supplement
- S029
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MYNX VASCULAR CLOSURE DEVICE
- Generic name
- Device, hemostasis, vascular
- Applicant
- Cordis US Corporation
- Date received
- 2010-03-29
- Decision date
- 2010-04-28
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- MGB
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Miami Lakes, FL
- Statement
- ADDING A MANUFACTURING PROCESS FOR THE ADVANCER TUBE COMPONENT IN-HOUSE.
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