FDA 510(k), K073164, IVS TUNNELLER DEVICES

FDA 510(k), K073164, IVS TUNNELLER DEVICES

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510(K) Number: K073164
Device Name: IVS TUNNELLER DEVICES
Manufacturer: SHARON ALEXANDER
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 11/09/2007
Date Received: 03/05/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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