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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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6 records meeting your search criteria returned- Product Code: LWJ Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. MODULAR FEMORAL STEM PRESS-FIT PLASMA SP 09/22/2017
ZIMMER BIOMET, INC. MODULAR FEMORAL STEM PRESS-FIT PLASMA SP 09/22/2017
STRYKER ORTHOPAEDICS-MAHWAH C-TAPER COCR LFIT HEAD 28MM/0 07/13/2015
STRYKER ORTHOPAEDICS-MAHWAH 32MM +8 V40 TAPER VIT HEAD 12/09/2014
STRYKER ORTHOPAEDICS-MAHWAH C-TAPER COCR LFIT HEAD 32MM/+5 07/02/2014
STRYKER ORTHOPAEDICS-MAHWAH 32MM -4 V40 TAPER VIT HEAD 02/24/2014
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