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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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3 records meeting your search criteria returned- Product Code: MNH Product Problem: Malposition of Device Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
LIFE SPINE, INC. AVATAR 01/29/2021
GLOBUS MEDICAL, INC. CREO 11/25/2020
STRYKER SPINE-US XIA 3 TITANIUM BLOCKER 12/21/2017
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