VIBRANT SOUNDBRIDGE DIRECT DRIVE DEMONSTRATOR
FDA premarket approval P990052/S007 · decided 2002-04-17
Approval details
- PMA number
- P990052
- Supplement
- S007
- Supplement type
- Real-Time Process
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- VIBRANT SOUNDBRIDGE DIRECT DRIVE DEMONSTRATOR
- Generic name
- Implant, hearing, active, middle ear, partially implanted
- Applicant
- Med-El Elektromedizinische Gerate GmbH
- Date received
- 2002-02-01
- Decision date
- 2002-04-17
- Days to decision
- 75 days
- Decision code
- APPR
- Product code
- MPV
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Innsbruck
- Statement
- APPROVAL FOR THE ADDITION OF THE DIRECT DRIVE DEMONSTRATOR TO THE VIBRANT SOUNDBRIDGE SYSTEM. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME VIBRANT SOUNDBRIDGE DIRECT DRIVE DEMONSTRATOR. THE INDICATIONS FOR USE FOR THE DEVICE HAVE NOT CHANGED.
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