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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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82 records meeting your search criteria returned- Product Code: NEK Patient Problem: Seroma Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 02/15/2024
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 12/19/2023
MEDTRONIC SOFAMOR DANEK USA, INC. MEDTRONIC SPINAL GRAFT TECH T FIBERCELL 05/28/2021
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 09/17/2018
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 07/25/2018
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 03/01/2018
MEDTRONIC INC. INFUSE RHBMP - 2 01/02/2018
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 11/20/2017
MEDTRONICS INFUSE WITH CAGE 04/11/2017
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 02/21/2017
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