PMA P960040S393
- Device
- TELIGEN, ENERGEN, PUNCTUA, INCEPTA, ORIGEN, INOGEN, DYNAGEN, AUTOGEN, PERCIVA, RESONATE, MOMENTUM, VIGILANT
- Applicant
- Boston Scientific
- PMA number
- P960040
- Supplement
- S393
- Product code
- LWS
- Decision date
- 2017-08-07
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- Approval for the LATITUDE NXT Release 5.0.1 Communicator software to add support for an alternative cellular adapter.
Current openFDA PMA Record#
- Device
- TELIGEN, ENERGEN, PUNCTUA, INCEPTA, ORIGEN, INOGEN, DYNAGEN, AUTOGEN, PERCIVA, RESONATE, MOMENTUM, VIGILANT
- Applicant
- Boston Scientific
- PMA number
- P960040
- Supplement
- S393
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2017-08-07
- Decision code
- APPR
- Date received
- 2017-05-22
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- Approval for the LATITUDE NXT Release 5.0.1 Communicator software to add support for an alternative cellular adapter.