PMA P040044S045
- Device
- MYNX VASCULAR CLOSURE DEVICE
- Applicant
- Cordis US Corporation
- PMA number
- P040044
- Supplement
- S045
- Product code
- MGB
- Decision date
- 2013-07-22
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED IN SANTA CLARA, CALIFORNIA.
Current openFDA PMA Record#
- Device
- MYNX VASCULAR CLOSURE DEVICE
- Applicant
- Cordis US Corporation
- PMA number
- P040044
- Supplement
- S045
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2013-07-22
- Decision code
- APPR
- Date received
- 2012-11-14
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED IN SANTA CLARA, CALIFORNIA.