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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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9 records meeting your search criteria returned- Product Code: KWY Product Problem: No Apparent Adverse Event Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US BI MENTUM PFRK PE LINER 22 45 06/16/2022
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 4 NON-CEMENTED 04/12/2022
DEPUY ORTHOPAEDICS INC US LPS CEM FEM STEM 13X150MM BOW 07/15/2020
DEPUY ORTHOPAEDICS INC US SELF CENT HIP 48X28 BRN 12/10/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR LINERS 04/18/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL HEAD 04/16/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 04/16/2019
ZIMMER BIOMET, INC. UNKNOWN BIOMET INTERGRAL 180, PRIMARY ST 05/09/2018
ZIMMER GMBH BIOLOX DELTA, CERAMIC FEMORAL HEAD, L¸ 4 07/05/2016
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