PMA P240011S008
- Device
- Altaviva™
- Applicant
- Medtronic Neuromodulation
- PMA number
- P240011
- Supplement
- S008
- Product code
- QPT
- Decision date
- 2026-02-27
- Classification
- Gastroenterology, Urology
- Generic name
- Stimulator, tibial, electrical, implantable, for urinary incontinence
- Approval order statement
- to implement a new Keyence Inspection System for the battery electrode compression process set-up
Current openFDA PMA Record#
- Device
- Altaviva™
- Applicant
- Medtronic Neuromodulation
- PMA number
- P240011
- Supplement
- S008
- Product code
- QPT
- Generic name
- Stimulator, tibial, electrical, implantable, for urinary incontinence
- Decision date
- 2026-02-27
- Decision code
- OK30
- Date received
- 2026-01-30
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- to implement a new Keyence Inspection System for the battery electrode compression process set-up