PMA P970013S096
- Device
- Microny family of Pacemakers
- Applicant
- ABBOTT MEDICAL
- PMA number
- P970013
- Supplement
- S096
- Product code
- LWO
- Decision date
- 2025-02-05
- Classification
- Cardiovascular
- Generic name
- Pulse-generator, single chamber, sensor driven, implantable
- Approval order statement
- approval for a model expansion of the NGQ Family of CRT-Ds with new header configurations
Current openFDA PMA Record#
- Device
- Microny family of Pacemakers
- Applicant
- ABBOTT MEDICAL
- PMA number
- P970013
- Supplement
- S096
- Product code
- LWO
- Generic name
- Pulse-generator, single chamber, sensor driven, implantable
- Decision date
- 2025-02-05
- Decision code
- APPR
- Date received
- 2024-09-17
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- approval for a model expansion of the NGQ Family of CRT-Ds with new header configurations