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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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5 records meeting your search criteria returned- Product Code: IKD Patient Problem: Insufficient Information Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
A&E MEDICAL CORP. STERNALOCK CABLE FIXATION 08/15/2023
PHILIPS NORTH AMERICA LLC UNKNOWN MEDICAL CONSUMABLES AND SENSORS 09/24/2022
COVIDIEN LLC CABLE, ELECTRODE 08/25/2021
ALPHATEC SPINE, INC. SAFEOP 06/17/2021
GE HEALTHCARE FINLAND OY GE 01/06/2021
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