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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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86 records meeting your search criteria returned- Product Code: KWQ Product Problem: Unintended Movement Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SYNTHES USA 4.0MM TI CANCELLOUS BONE SCREW SELF-TAPP 04/27/2016
NUVASIVE, INC. NUVASIVE HELIX REVOLUTION ACP SYSTEM 04/12/2016
NUVASIVE, INC. NUVASIVE TRAVERSE PLATE SYSTEM 04/05/2016
SYNTHES USA 4.35MM TI CANCELLOUS EXP HEAD SCREW/SELF 03/22/2016
SYNTHES USA APPLIANCE, FIXATION, SPINAL INTERVERTEBR 12/14/2015
SYNTHES USA APPLIANCE, FIXATION, SPINAL INTERVERTEBR 12/11/2015
SYNTHES USA APPLIANCE, FIXATION, SPINAL INTERVERTEBR 12/11/2015
SYNTHES USA 1.8MM TI LOCKING SCREW 11/24/2015
SYNTHES USA 1.8MM TI LOCKING SCREW 11/24/2015
SYNTHES USA 1.8MM TI LOCKING SCREW 11/24/2015
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