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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
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4 records meeting your search criteria returned- Product Code: PBI Patient Problem: Weakness Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. G7 OSSEOTI MULTIHOLE 50MM D 07/15/2019
ZIMMER BIOMET, INC. G7 HI-WALL E1 LINER 36MM D 07/15/2019
BIOMET ORTHOPEDICS G7 NEUTRAL ARCOMXL LINER 07/07/2017
BIOMET ORTHOPEDICS G7 PPS LTD ACET SHELL 54F 06/02/2016
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