PMA P040044S053
- Device
- MYNX CADENCE AND MYNXGRIP VASCULAR CLOSURE DEVICES
- Applicant
- Cordis US Corporation
- PMA number
- P040044
- Supplement
- S053
- Product code
- MGB
- Decision date
- 2014-05-01
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- IMPLEMENTATION OF A DIFFERENT STERILIZATION CONFIGURATION FOR THE MYNX® PRODUCT FAMILY OF DEVICES.
Current openFDA PMA Record#
- Device
- MYNX CADENCE AND MYNXGRIP VASCULAR CLOSURE DEVICES
- Applicant
- Cordis US Corporation
- PMA number
- P040044
- Supplement
- S053
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2014-05-01
- Decision code
- OK30
- Date received
- 2014-04-01
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- IMPLEMENTATION OF A DIFFERENT STERILIZATION CONFIGURATION FOR THE MYNX® PRODUCT FAMILY OF DEVICES.