BRAVA CRT-D, VIVA S CRT-D, VIVA XT CRT-D IPG
FDA premarket approval P010031/S407 · decided 2013-12-17
Approval details
- PMA number
- P010031
- Supplement
- S407
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- BRAVA CRT-D, VIVA S CRT-D, VIVA XT CRT-D IPG
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2013-11-18
- Decision date
- 2013-12-17
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- MODIFICATION TO THE BATTERY HEADER WELD POWER RANGE.
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