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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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8 records meeting your search criteria returned- Product Code: LOE Patient Problem: No Code Available Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
EBI, LLC. SPF-PLUS 60/M 09/02/2020
EBI, LLC. SPF-XL IIB 2/DM 08/05/2020
BIOCOMPOSITES LTD STIMULAN 12/23/2019
EBI, LLC. SPF-PLUS 60/M 08/29/2017
EBI, LLC. SPF SPINAL FUSION STIMULATOR 07/06/2017
EBI, LLC. EBI SPF IMPLANTABLE SPINAL FUSION STIMUL 03/29/2017
BIOMET SPINE - BROOMFIELD SPF-PLUS IMPLANTABLE STIMULATOR 08/25/2016
BIOMET SPINAL PAK 11/18/2014
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