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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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7 records meeting your search criteria returned- Product Code: MAX Product Problem: Device Issue Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
LIFE SPINE LIFE SPINE 02/01/2018
MEDACTA INTERNATIONAL SA MECTALIF OBLIQUE INTERBODY FUSION DEVICE 01/10/2018
MEDACTA INTERNATIONAL SA MECTALIF POSTERIOR INTERBODY FUSION DEVI 12/06/2017
MEDACTA INTERNATIONAL SA MECTALIF POSTERIOR INTERBODY FUSION DEVI 11/24/2017
SEASPINE, INC INTERBODY SYSTEM 02/16/2017
NUVASIVE, INC. AP EXPANDABLE XLIF SYSTEM 11/30/2016
AESCULAP AG A-SPACE SIBD BONE SCREW 4.5X30MM 06/01/2016
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