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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: NQO Patient Problem: No Information Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
PARADIGM SPINE GMBH COFLEX INTERLAMINAR TECHNOLOGY 02/27/2020
PARADIGM SPINE GMBH COFLEX INTERLAMINAR TECHNOLOGY 02/16/2018
PARADIGM SPINE GMBH COFLEX INTERLAMINAR TECHNOLOGY 11/17/2017
PARADIGM SPINE GMBH COFLEX INTERLAMINAR TECHNOLOGY 01/19/2016
MEDTRONIC SOFAMOR DANEK USA, INC X-STOP PEEK INTERSPINOUS SPACER 05/18/2015
MEDTRONIC SOFAMOR DANEK X-STOP®PEEK INTERSPINOUS SPACER 09/10/2014
MDT KYPHON SUNNYVALE MFG X-STOP PEEK INTERSPINOUS SPACER 02/26/2014
MDT KYPHON SUNNYVALE MFG X-STOP PEEK INTERSPINOUS SPACER 02/13/2014
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