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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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186 records meeting your search criteria returned- Product Code: MAI Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US UNK - IMPLANTS 10/28/2019
DEPUY MITEK LLC US UNK - IMPLANTS 10/24/2019
DEPUY MITEK LLC US 4.75 HEALIX ADVANCE KNTLSS BR 09/06/2019
MEDOS INTERNATIONAL SàRL INTRAFX ADVBR SCW9X30 W/LGSHTH 08/16/2019
DEPUY MITEK LLC US 5.5 HEALIX TI ANCHOR W/OCORD 07/31/2019
DEPUY MITEK LLC US UNKNOWN RIGIDFIX CROSS PIN 07/22/2019
DEPUY MITEK LLC US LUPINE BR DS W/ORTHCRD 07/18/2019
DEPUY MITEK LLC US 4.5 HEALIX ADVANCE BR3SUT W/OC 07/03/2019
DEPUY MITEK LLC US 4.5 HEALIX ADVANCE BR3SUT W/OC 07/03/2019
ARTHREX, INC. BIO-INTERF SCRW,FULL THD 7X 28MM 06/26/2019
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