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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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21 records meeting your search criteria returned- Product Code: KKY Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION HTR * PMI WALLRAVEN LEFT FRONTAL SPHENOI 04/03/2018
BIOMET MICROFIXATION HTR-PMI HASEWINKEL LEFT FRONTAL SPHENOID 03/12/2018
BIOMET MICROFIXATION HTR*PMI WALSH RIGHT FRONTAL PARIETAL TEM 01/22/2018
BIOMET MICROFIXATION HTR-PMI KOVALIOVAS LEFT FRONTAL SPHENOID 12/12/2017
BIOMET MICROFIXATION HTR-PMI KOVALIOVAS RIGHT FRONTAL SPHENOI 12/12/2017
BIOMET MICROFIXATION HTR-PMI RIGHT FRONTAL SPHENOID PARIETAL 11/13/2017
BIOMET MICROFIXATION HARD TISSUE REPLACE(HTR(R))-PATIENT-MATC 10/26/2017
BIOMET MICROFIXATION HARD TISSUE REPLACEMENT; RIGHT FRONTAL S 07/28/2016
BIOMET MICROFIXATION HTR-PMI RIGHT FRONTAL SPHENOID PARIETAL 12/16/2015
BIOMET MICROFIXATION HARD TISSUE REPLACEMENT -PATIENT MATCHED 08/04/2015
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