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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name mesh, surgical, polymeric
510(k) Number K073164
Device Name IVS TUNNELLER DEVICES
Original Applicant
COVIDIEN UK MANUFACTURING LTD
60 middletown avenue
north haven,  CT  06473
Original Contact sharon alexander
Regulation Number878.3300
Classification Product Code
FTL  
Date Received11/09/2007
Decision Date 03/05/2008
Decision substantially equivalent (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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