PMA P050023S192
- Device
- Renamic Neo
- Applicant
- Biotronik, Inc.
- PMA number
- P050023
- Supplement
- S192
- Product code
- MRM
- Decision date
- 2025-04-03
- Classification
- Cardiovascular
- Generic name
- DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
- Approval order statement
- approval for hardware updates to the Renamic Neo programmer
Current openFDA PMA Record#
- Device
- Renamic Neo
- Applicant
- Biotronik, Inc.
- PMA number
- P050023
- Supplement
- S192
- Product code
- MRM
- Generic name
- DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
- Decision date
- 2025-04-03
- Decision code
- APPR
- Date received
- 2025-01-10
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- approval for hardware updates to the Renamic Neo programmer