PMA P220012S072
- Device
- Aurora EV-ICD
- Applicant
- Medtronic, Inc.
- PMA number
- P220012
- Supplement
- S072
- Product code
- LWS
- Decision date
- 2026-04-30
- Classification
- Cardiovascular
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- to expand the electrolyte salt acceptance limits
Current openFDA PMA Record#
- Device
- Aurora EV-ICD
- Applicant
- Medtronic, Inc.
- PMA number
- P220012
- Supplement
- S072
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2026-04-30
- Decision code
- OK30
- Date received
- 2026-04-02
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- to expand the electrolyte salt acceptance limits