VENTAK MINI II+ HE, MINI IV, MINI IV+ PULSE GENERATORS
FDA premarket approval P910077/S056 · decided 2006-05-01
Approval details
- PMA number
- P910077
- Supplement
- S056
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VENTAK MINI II+ HE, MINI IV, MINI IV+ PULSE GENERATORS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2005-11-22
- Decision date
- 2006-05-01
- Days to decision
- 160 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- APPROVAL FOR AN UPDATE THE VISUAL INSPECTION CRITERIA IN GMAI (GENERAL MANUFACTURING AREA INSTRUCTION) I00093.
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