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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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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 - IMPLANT 10/28/2020
DEPUY MITEK LLC US GRYPHON P BR DS ANCHOR W/OC 10/20/2020
DEPUY MITEK LLC US GRYPHON P BR DS ANCHOR W/OC 10/20/2020
DEPUY MITEK LLC US UNK - IMPLANT 10/19/2020
DEPUY MITEK LLC US MINILOK QA+ # 2-0 OC V5 10/19/2020
DEPUY MITEK LLC US UNK - IMPLANT 09/22/2020
DEPUY MITEK LLC US 5.5 HEALIX3 PEEK ANC.W/OCORD 08/28/2020
DEPUY MITEK LLC US 4.75 HEALIX ADVANCE KNTLSS BR 07/24/2020
DEPUY MITEK LLC US GRYPHON PEEK W/PROKNOT 07/24/2020
DEPUY MITEK LLC US 4.5 HEALIX ADVANCE BR3SUT W/OC 06/26/2020
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