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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI INS SZ3 7MM RM/LL 05/24/2021
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI INS SZ4 8MM LM/RL 05/18/2021
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI TIB TRAY SZ3 LMRL 05/17/2021
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI INS SZ3 7MM LM/RL 05/17/2021
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI FEMORAL SZ3 LM/RL 05/17/2021
MICROPORT ORTHOPEDICS INC. EVOLUTIONMP FEM CS/CR NON-POR SIZE 2 PRI 05/17/2021
DEPUY ORTHOPAEDICS INC US PRSVN ALLPOLY TIB LM/RL S4 7MM 05/12/2021
ZIMMER BIOMET, INC. UNKNOWN OXFORD FEMORAL 05/12/2021
BIOMET UK LTD. UNK OXFORD BEARING COMPONENT 05/05/2021
BIOMET UK LTD. UNK OXFORD FEMORAL COMPONENT 05/05/2021
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