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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
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9 records meeting your search criteria returned- Product Code: LOE Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET SPINE INC. EBI SPF-XL IIB BONE GROWTH STIMULATOR 05/03/2019
EBI, LLC. SPF-PLUS 60/M 05/01/2019
EBI, LLC. OSTEOGEN-20/M SURGICALLY IMPLANTED BONE 03/26/2019
EBI, LLC. OSTEOGEN-20/M SURGICALLY IMPLANTED BONE 03/26/2019
EBI, LLC. SPF-PLUS 60/M 03/04/2019
EBI, LLC. EBI OSTEOGEN-20/M BONE GROWTH STIMULATOR 11/28/2018
BIOMET SPINE - BROOMFIELD SPF-PLUS IMPLANTABLE STIMULATOR 08/25/2016
BIOMET SPINE - BROOMFIELD SPF-XL IIB 2/DM IMPLANTABLE STIMULATOR 12/18/2015
EBI, LLC. SPF SPINAL FUSION STIMULATOR 01/17/2014
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