PMA P990001S056
- Device
- CLARITY DDDR, CLARITY SSIR, DIAMOND III, RUBY III, TOPAZ III, JADE III, VITA 2 DDDR, C-SERIES, AND T-SERIES FAMILY OF IP
- Applicant
- Medtronic, Inc.
- PMA number
- P990001
- Supplement
- S056
- Product code
- NVZ
- Decision date
- 2009-10-08
- Generic name
- Pulse generator, permanent, implantable
- Approval order statement
- CHANGE IN LOCATION OF A STERILIZATION SYSTEM.
Current openFDA PMA Record
- Device
- CLARITY DDDR, CLARITY SSIR, DIAMOND III, RUBY III, TOPAZ III, JADE III, VITA 2 DDDR, C-SERIES, AND T-SERIES FAMILY OF IP
- Applicant
- Medtronic, Inc.
- PMA number
- P990001
- Supplement
- S056
- Product code
- NVZ
- Generic name
- Pulse generator, permanent, implantable
- Decision date
- 2009-10-08
- Decision code
- OK30
- Date received
- 2009-09-08
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE IN LOCATION OF A STERILIZATION SYSTEM.