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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
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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100 records meeting your search criteria returned- Product Code: JDI Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS UNKNOWN HIP 04/07/2015
BIOMET ORTHOPEDICS M/H RADIAL 3-HOLE SHELL 54MM 03/20/2015
BIOMET ORTHOPEDICS 28MM DIA COCR MOD HD -3MM NK 03/20/2015
BIOMET ORTHOPEDICS ARCOM 28MM RNGLOC LNR 10DEG25 03/20/2015
BIOMET ORTHOPEDICS TAPERLOC MICROP FMRL 5.0MM 03/20/2015
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_CORK_PRODUCT 03/17/2015
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RECONSTRUCTIVE_PRODUCT 02/20/2015
STRYKER ORTHOPAEDICS-MAHWAH 28MM -4 LFIT V40 HEAD 02/17/2015
BIOMET ORTHOPEDICS 36MM COCR MOD HD +3MM 02/17/2015
BIOMET ORTHOPEDICS EPOLY 36MM RLC LNR +5 SZ23 02/12/2015
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