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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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17 records meeting your search criteria returned- Product Code: LXH Product Problem: Failure to Eject Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. BURR ATTACHMENT 2.35 MM 01/03/2024
K2M, INC. SCREW INSERTER 10/29/2022
K2M, INC. MI OFFSET ROD REDUCER 08/08/2022
K2M, INC. PROVISIONAL SPLIT DRIVER; SIZE 30 08/01/2022
K2M, INC. SCREW INSERTER 07/29/2022
K2M, INC. SCREW INSERTER 04/29/2022
K2M, INC. SCREW INSERTER 01/27/2022
K2M, INC. NAVIGATED SCREW INSERTER; YUKON 01/26/2022
K2M, INC. NAVIGATED CERVICAL SCREW INSERTER; YUKON 01/26/2022
MEDTRONIC SOFAMOR DANEK USA, INC LONGITUDE II 09/14/2020
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