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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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56 records meeting your search criteria returned- Product Code: JDR Patient Problem: Not Applicable Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US SUPER QA+ O/C DS CP-2 *EA 10/21/2020
DEPUY MITEK LLC US GII QA+ #2 PAN CP-2 *EA 10/03/2020
DEPUY MITEK LLC US GII QA+ #2 ETH CP-2 *EA 09/21/2020
DEPUY MITEK LLC US GII QA+ #2 ETH CP-2 *EA 09/21/2020
DEPUY MITEK LLC US GII QA+ #2 ETH CP-2 *EA 09/21/2020
DEPUY MITEK LLC US GII QA+ #2 ETH CP-2 *EA 09/11/2020
DEPUY MITEK LLC US GII QA+ #2 ETH CP-2 *EA 09/11/2020
DEPUY MITEK LLC US GII QA+ #2 ETH CP-2 *EA 08/24/2020
DEPUY MITEK LLC US MINI QA+ #2/O OCORD V-5 07/23/2020
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 01/30/2020
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