VITALITY & VITALITY 2 DEVICE FAMILY
FDA premarket approval P960040/S160 · decided 2008-02-13
Approval details
- PMA number
- P960040
- Supplement
- S160
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- VITALITY & VITALITY 2 DEVICE FAMILY
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2008-01-17
- Decision date
- 2008-02-13
- Days to decision
- 27 days
- Decision code
- APPR
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- APPROVAL TO ADD WARNING INFORMATION REGARDING CORRECT DEVICE IMPLANT ORIENTATION TO THE LABELING OF THE DEVICES.
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