PMA P990001S083
- Device
- VITATRON DA+C-SERIES/VITATRON DA+T SERIES
- Applicant
- Medtronic, Inc.
- PMA number
- P990001
- Supplement
- S083
- Product code
- NVZ
- Decision date
- 2011-02-24
- Generic name
- Pulse generator, permanent, implantable
- Approval order statement
- REVISION OF PARAMETERS TO AN EPOXY DISPENSE MANUFACTURING PROCESS.
Current openFDA PMA Record
- Device
- VITATRON DA+C-SERIES/VITATRON DA+T SERIES
- Applicant
- Medtronic, Inc.
- PMA number
- P990001
- Supplement
- S083
- Product code
- NVZ
- Generic name
- Pulse generator, permanent, implantable
- Decision date
- 2011-02-24
- Decision code
- OK30
- Date received
- 2011-01-25
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- REVISION OF PARAMETERS TO AN EPOXY DISPENSE MANUFACTURING PROCESS.