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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
ZIMMER BIOMET, INC. NEXGEN PROVISIONAL STEMMED TIBIAL COMPON 04/01/2019
MICROPORT ORTHOPEDICS INC. ACETABULAR CUP 03/05/2019
ZIMMER BIOMET, INC. PROV LINER ELEVATED MM 36 02/25/2019
ZIMMER BIOMET, INC. DISCOVERY PROV LOCK SCREW 01/23/2019
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE CD 20 01/15/2019
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE CD 12 01/15/2019
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE CD 14 01/15/2019
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE EF 14 01/15/2019
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE CD 17 01/15/2019
ZIMMER BIOMET, INC. PROVISIONAL LINER 28 MM I.D. FOR USE WIT 12/07/2018
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