TRILOGY/SOLUS II/PARAGON III/PHOENIX III/SYNCHRONY II,III/ ADDVENT TEMPO
FDA premarket approval P900070/S026 · decided 2000-02-18
Approval details
- PMA number
- P900070
- Supplement
- S026
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- TRILOGY/SOLUS II/PARAGON III/PHOENIX III/SYNCHRONY II,III/ ADDVENT TEMPO
- Generic name
- Programmer, pacemaker
- Applicant
- St. Jude Medical, Cardiac Rhythm Management Divisi
- Date received
- 2000-01-31
- Decision date
- 2000-02-18
- Days to decision
- 18 days
- Decision code
- OK30
- Product code
- KRG
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- The 30-day notice requested the elimination of in-process x-ray imaging for all bradycardia pulse generators.
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