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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
7 records meeting your search criteria returned- Product Code: KWY Patient Problem: Muscle/Tendon Damage Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ZB 12/14 COCR FRDM 36MM X +6 01/25/2022
ZIMMER BIOMET, INC. ZB 12/14 COCR FRDM 36MM X +6 12/01/2021
STRYKER ORTHOPAEDICS / HOWMEDICA OSTEONI STRYKER ORTHOPAEDICS-MAHWAH ABGII NO5 CE 05/10/2021
STRYKER ORTHOPAEDICS / HOWMEDICA OSTEONI STRYKER ORTHOPAEDICS-MAHWAH ABGII NO5 CE 05/10/2021
ZIMMER BIOMET, INC. UNKNOWN STEM 01/04/2021
DEPUY ORTHOPAEDICS INC US UNK HIP FEMORAL HEAD METAL 07/16/2019
DEPUY INTERNATIONAL LTD - 8010379 UNK HIP FEMORAL HEAD METAL ASR 12/14/2018
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