VENTAK P
FDA premarket approval P890061/S016 · decided 2004-12-22
Approval details
- PMA number
- P890061
- Supplement
- S016
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VENTAK P
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2004-12-03
- Decision date
- 2004-12-22
- Days to decision
- 19 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- USE OF A NEW BIOLOGICAL INDICATOR FOR THE STERILIZATION PROCESS.
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