PMA P050023S206
- Device
- TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD
- Applicant
- Biotronik, Inc.
- PMA number
- P050023
- Supplement
- S206
- Product code
- MRM
- Decision date
- 2026-02-03
- Classification
- Cardiovascular
- Generic name
- DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
- Approval order statement
- removal of redundant incoming inspection from certain qualified suppliers
Current openFDA PMA Record#
- Device
- TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD
- Applicant
- Biotronik, Inc.
- PMA number
- P050023
- Supplement
- S206
- Product code
- MRM
- Generic name
- DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
- Decision date
- 2026-02-03
- Decision code
- OK30
- Date received
- 2026-01-14
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- removal of redundant incoming inspection from certain qualified suppliers