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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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51 records meeting your search criteria returned- Product Code: KWD Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
TRILLIANT SURGICAL 3S HEMI STERILE IMPLANT - SMALL 11/02/2018
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 03/30/2018
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 03/28/2018
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 12/26/2017
ARTHREX INC. ANATOEMIC, 18.5MM 11/21/2017
ARTHROSURFACE, INC. HEMICAP® MTP RESURFACING HEMI-ARTHROPLAS 10/25/2017
ARTHROSURFACE, INC. CAP GREAT TOE RESURFACING HEMI-ARTHROPLA 10/17/2017
ASCENSION ORTHOPEDICS MGT MOVEMENT PROX. PHAL. TOTAL SZ. 40 01/13/2016
ARTHROSURFACE CAP 7.0MM MTP RESURFACING HEMI-ARTHROPLA 11/18/2015
ASCENSION ORTHOPEDICS, INC. MGT MOVEMENT METATARSAL SZ. 20 02/10/2015
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