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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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97 records meeting your search criteria returned- Product Code: KWL Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. TPRLC 133 MP TYPE1 PPS SO 18.0 11/21/2022
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS HO 11X142MM 2MM T1 03/14/2022
ZIMMER BIOMET, INC. TPRLC 133 FP TYPE1 PPS SO 7.0 12/01/2021
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 9 12/29/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 2 12/17/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 9 11/30/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 11/24/2020
DEPUY ORTHOPAEDICS INC US ACTIS COLLARED HIGH SIZE 7 11/23/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 6 10/30/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 09/11/2020
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