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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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13 records meeting your search criteria returned- Product Code: JDK Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US BIOSTOP G CEM RESTR 12MM 02/15/2024
DEPUY ORTHOPAEDICS INC US CEMENTRALIZER 11.0 02/13/2024
DEPUY ORTHOPAEDICS INC US CEMENTRALIZER 12.0 12/06/2023
DEPUY ORTHOPAEDICS INC US CEMENTRALIZER 12.0 11/08/2023
DEPUY INTERNATIONAL LTD - 8010379 CEMENTRALIZER 13.0 09/26/2023
DEPUY ORTHOPAEDICS INC US CEMENTRALIZER 10.0MM 03/11/2022
DEPUY ORTHOPAEDICS INC US CEMENTRALIZER 10.0MM 04/15/2021
DEPUY ORTHOPAEDICS INC US CEMENTRALIZER 10.0MM 11/13/2020
DEPUY CMW - 9610921 CEMENT RESTRICTOR SIZE 4 12/23/2019
DEPUY ORTHOPAEDICS INC US CEMENT RESTRICTOR SIZE 4 11/22/2019
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