CLARION DEVICE FITTING SOFTWARE (SCLIN)
FDA premarket approval P960058/S010 · decided 1999-07-16
Approval details
- PMA number
- P960058
- Supplement
- S010
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- CLARION DEVICE FITTING SOFTWARE (SCLIN)
- Applicant
- Advanced Bionics
- Date received
- 1999-03-24
- Decision date
- 1999-07-16
- Days to decision
- 114 days
- Decision code
- APPR
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Valencia, CA
- Statement
- Approval for the modifications to the Device Fitting Software for adults and pediatrics. The device, as modified, will be marketed under the trade name Clarion Multi-Strategy Cochlear Implant (Adult) and (Pediatrics) and is indicated to restore a level of auditory sensation to individuals with profound sensorineural deafness via electrical stimulation of the auditory nerve.
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