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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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99 records meeting your search criteria returned- Product Code: JDI Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS 28MM DIA COCR MOD HD -3MM NK 08/05/2014
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_CORK_PRODUCT 08/01/2014
BIOMET ORTHOPEDICS E-POLY 40MM +3 HIWALL LNR SZ24 07/23/2014
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM/+5 07/16/2014
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RECONSTRUCTIVE_PRODUCT 07/10/2014
BIOMET ORTHOPEDICS UNKNOWN HIP 07/07/2014
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RECONSTRUCTIVE_PRODUCT 06/26/2014
STRYKER ORTHOPAEDICS-MAHWAH 32MM -4 LFIT V40 HEAD 06/25/2014
BIOMET ORTHOPEDICS RAN/BUR RNGLC SHL 60MM SZ 25 06/16/2014
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM/+5 06/03/2014
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