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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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4 records meeting your search criteria returned- Product Code: HTY Product Problem: Insufficient Information Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS UNKNOWN PIN 04/12/2017
BIOMET TRAUMA UNKNOWN TRAUMA 08/18/2016
BIOMET TRAUMA UNKNOWN TRAUMA 08/18/2016
STRYKER GMBH (MDR) UNKNOWN_SELZACH_PRODUCT 06/03/2015
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