LATITUDE NXT Remote Patient Management System, LATITUDEWave Communicator, LATITUDE Consult Communicator, LATITUDE NX
FDA premarket approval P910077/S185 · decided 2021-09-17
Approval details
- PMA number
- P910077
- Supplement
- S185
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- LATITUDE NXT Remote Patient Management System, LATITUDEWave Communicator, LATITUDE Consult Communicator, LATITUDE NX
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2021-06-21
- Decision date
- 2021-09-17
- Days to decision
- 88 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Approval for the software modifications to the LATITUDE NXT Remote Patient Management System.
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