LATITUDE Programming System
FDA premarket approval P910077/S172 · decided 2019-07-08
Approval details
- PMA number
- P910077
- Supplement
- S172
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- LATITUDE Programming System
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2019-04-10
- Decision date
- 2019-07-08
- Days to decision
- 89 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Approval to modify the Model 3300 LATITUDE Programming System software components.
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