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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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38 records meeting your search criteria returned- Product Code: KKY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION HTR*PMI 2025734 LEFT FRONTAL TEMPORAL PA 08/31/2020
BIOMET MICROFIXATION HTR PMI BURGER RIGHT TEMPORAL PARIETAL I 06/22/2020
PORIFEROUS, LLC SU-POR SURGICAL IMPLANTS 03/13/2020
BIOMET MICROFIXATION HTR-PMI A.B. 1953-20190619 RIGHT TOP PAR 02/13/2020
BIOMET MICROFIXATION HTR-PMI G.S.1958 RIGHT FRONTAL PARIETAL 08/09/2019
OXFORD PERFORMANCE MATERIALS HTR-PEKK 03/26/2019
OXFORD PERFORMANCE MATERIALS HTR-PEKK 03/26/2019
BIOMET MICROFIXATION HTR-PMI PACIENTE 2 BI-FRONTAL RIGHT IMPL 03/06/2019
BIOMET MICROFIXATION HTR-PMI PACIENTE 1 BI-FRONTAL ORBITAL IM 03/06/2019
MATRIX SURGICAL USA OMNIPORE SURGICAL IMPLANT - TWO-PIECE CH 02/07/2019
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