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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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130 records meeting your search criteria returned- Product Code: JDL Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. CONSERVE(R) TOTAL A-CLASS(R) FEMORAL HEA 02/02/2016
MICROPORT ORTHOPEDICS INC. CONSERVE TOTAL A-CLASS FEMORAL HEAD W/ B 01/30/2016
MICROPORT ORTHOPEDICS INC. LINEAGE(R) TRANSCEND(R) SUPERFINISHED FE 01/29/2016
MICROPORT ORTHOPEDICS INC. LINEAGE(R) TRANSCEND(R) SUPERFINISHED FE 01/16/2016
MICROPORT ORTHOPEDICS INC. LINEAGE(R) TRANSCEND(R) SUPERFINISHED FE 01/05/2016
MICROPORT ORTHOPEDICS INC. LINEAGE(R) TRANSCEND(R) SUPERFINISHED FE 12/03/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) TOTAL A-CLASS HEAD 12/03/2015
MICROPORT ORTHOPEDICS INC. WRIGHT HIP 11/25/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) TOTAL A-CLASS(R) HEAD W/BFH 05/28/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) TOTAL A-CLASS HEAD 05/21/2015
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