MYNX VASCULAR CLOSURE DEVICE
FDA premarket approval P040044/S020 · decided 2009-11-20
Approval details
- PMA number
- P040044
- Supplement
- S020
- 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
- 2009-10-22
- Decision date
- 2009-11-20
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- MGB
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Miami Lakes, FL
- Statement
- MODIFICATION OF AN IN-PROCESS TEST TO EVALUATE MOISTURE CONTENT OF THE SEALANT IN THE MYNX DEVICE.
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