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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 4.75 HEALIX ADVANCE KNTLSS BR 02/06/2019
DEPUY MITEK LLC US 4.75 HEALIX ADVANCE KNTLSS BR 02/06/2019
DEPUY MITEK LLC US GRYPHON P BR DS ANCHOR W/OC 02/05/2019
DEPUY MITEK LLC US 5.5 HEALIX ADVANCE KNTLSS BR 01/30/2019
DEPUY MITEK LLC US MILAGRO ADVANCE SCREW 7X23MM 01/28/2019
DEPUY MITEK LLC US MICROFIX QA+#3/0 OC V-4W/BIT 01/25/2019
DEPUY MITEK LLC US GRYPHON P BR W PERMACORD 01/23/2019
DEPUY MITEK LLC US GRYPHON P BR W PERMACORD 01/23/2019
DEPUY MITEK LLC US MINILOK QA+ #2-0 ETH V-5 W/BIT 01/23/2019
DEPUY MITEK LLC US MINILOK QA+ #2-0PAN RB-1 W/BIT 01/22/2019
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