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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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213 records meeting your search criteria returned- Product Code: NRA Product Problem: Loose or Intermittent Connection Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN KNEE 10/13/2017
ZIMMER BIOMET, INC. UNKNOWN KNEE 10/13/2017
ZIMMER BIOMET, INC. UNKNOWN KNEE 10/13/2017
ZIMMER BIOMET, INC. UNKNOWN KNEE 10/09/2017
ZIMMER BIOMET, INC. UNKNOWN KNEE 10/09/2017
ZIMMER BIOMET, INC. OXF ANAT BRG LT SM SIZE 3 PMA 10/05/2017
ZIMMER BIOMET, INC. OXF ANAT BRG RT SM SIZE 4 PMA 10/05/2017
BIOMET ORTHOPEDICS OXF TWIN-PEG CMNTD FEM MD PMA 02/08/2016
BIOMET UK LTD OXFORD UNI FEMORAL MD 02/03/2016
BIOMET ORTHOPEDICS OXFORD PKS COCR SIZE A RM STD 02/03/2016
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