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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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6 records meeting your search criteria returned- Product Code: MAX Product Problem: Defective Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MDT SOFAMOR DANEK PUERTO RICO MFG CAPSTONE VERTEBRAL BODY SPACER 08/24/2020
BENVENUE MEDICAL, INC. LUNA 3D 12/11/2018
AESCULAP IMPLANT SYSTEMS TSPACE XP IMPLANT 5° 30X11.5X11MM 03/08/2018
STRYKER SPINE-FRANCE AVS UNILIF SPACER 10 X 30 X 0DEG - 11MM 11/09/2016
AESCULAP AG AND CO. KG PROSPACE XP IMPLANT 5 DEGREE 10X10.5X22M 07/22/2015
ORTHOFIX INC. FORZA SPACER 06/16/2015
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