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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Prosthesis, Laryngeal (Taub)
510(k) Number K090455
Device Name PROVOX VEGA, MODEL 8130-8135
Applicant
ATOS MEDICAL AB
KRAFTGATAN 8
HORBY,  SE SE-24222
Applicant Contact FERENC DAHNER
Correspondent
ATOS MEDICAL AB
KRAFTGATAN 8
HORBY,  SE SE-24222
Correspondent Contact FERENC DAHNER
Regulation Number874.3730
Classification Product Code
EWL  
Date Received02/23/2009
Decision Date 06/05/2009
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Summary Summary
Type Traditional
Clinical Trials NCT00743262
NCT00884910
Reviewed by Third Party No
Combination Product No
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