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MULTI-STRATEGY COCHLEAR IMPLANT-PLATINUM BTE SOUND PROCESSOR (ADULT)

FDA premarket approval P940022/S016 · decided 2001-01-12

Approval details

PMA number
P940022
Supplement
S016
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MULTI-STRATEGY COCHLEAR IMPLANT-PLATINUM BTE SOUND PROCESSOR (ADULT)
Generic name
Implant, cochlear
Applicant
Advanced Bionics Corp.
Date received
2000-11-16
Decision date
2001-01-12
Days to decision
57 days
Decision code
APPR
Product code
MCM
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Sylmar, CA
Statement
APPROVAL FOR INCORPORATION OF THE SIZE-REDUCED SPEECH PROCESSOR TO BE WORN BEHIND THE EAR, KNOWN AS THE PLATINUM BTE(TM) SOUND PROCESSOR. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME CLARION(R) MULTI-STRATEGY COCHLEAR IMPLANT PLATINUM BTE SOUND PROCESSOR. THE DEVICE IS INDICATED TO RESTORE A LEVEL OF AUDITORY SENSATION TO INDIVIDUALS WITH PROFOUND SENSORINEURAL DEAFNESS VIA ELECTRICAL STIMULATION OF THE AUDITORY NERVE. ADULTS: 1) 18 YEARS OF AGE OR OLDER 2) PROFOUND, BILATERAL

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