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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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93 records meeting your search criteria returned- Product Code: KWY Product Problem: Break Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
LIMACORPORATE S.P.A. MODULUS-STRUM. - ESTRATTORE 08/26/2021
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 12/08/2020
DEPUY ORTHOPAEDICS, INC. BIPOLAR HIP ASSEMBLY 10/15/2020
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 3 NON-CEMENTED 07/11/2020
BIOMET UK LTD. RLOC-X E1 H/W +3MM 50/36MM 23 03/23/2020
DEPUY ORTHOPAEDICS INC US UNK ACETABULAR TRIAL 03/06/2020
Unknown Manufacturer FEMUR BONE 02/24/2020
DEPUY ORTHOPAEDICS INC US ZT TRIAL SLEEVE 20B SML 10/03/2019
DEPUY ORTHOPAEDICS INC US ZT TRIAL SLEEVE 16F SML 10/03/2019
BIOMET UK LTD. BI-POLAR 28 CUP 52MM 09/14/2019
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