VIBRANT SOUNDBRIDGE
FDA premarket approval P990052/S015 · decided 2006-12-13
Approval details
- PMA number
- P990052
- Supplement
- S015
- Supplement type
- Real-Time Process
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- VIBRANT SOUNDBRIDGE
- Generic name
- Implant, hearing, active, middle ear, partially implanted
- Applicant
- Med-El Elektromedizinische Gerate GmbH
- Date received
- 2006-11-24
- Decision date
- 2006-12-13
- Days to decision
- 19 days
- Decision code
- APPR
- Product code
- MPV
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Innsbruck
- Statement
- APPROVAL FOR A CHANGE IN THE WORDING OF THE INDICATIONS FOR USE STATEMENT AND A NEW PRODUCT CODE DESCRIPTION THAT REMOVES THE REFERENCE TO HEARING AIDS. THE DEVICE IS INDICATED FOR USE IN ADULTS, 18 YEARS OF AGE OR OLDER, WHO HAVE A MODERATE TO SEVERE SENSORINEURAL HEARING LOSS. PRIOR TO RECEIVING THE DEVICE, IT IS RECOMMENDED THAT AN INDIVIDUAL HAVE EXPERIENCE WITH APPROPRIATELY FIT HEARING AIDS.
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