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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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152 records meeting your search criteria returned- Product Code: NKB Product Problem: Malposition of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
MEDTRONIC SOFAMOR DANEK USA, INC. CD HORIZON SPINAL SYSTEM 10/03/2019
STRYKER SPINE-US UNKNOWN_SPINE_PRODUCT 05/22/2019
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA VOYAGER SPINAL SYSTEM 04/30/2019
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA VOYAGER SPINAL SYSTEM 04/30/2019
ALPHATEC SPINE INC CANNULATED EXTENDED TAB POLYAXIAL REDUCT 01/29/2019
MEDACTA INTERNATIONAL SA PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SC 10/31/2018
NUVASIVE INC. NUVASIVE PRECEPT SPINAL SYSTEM 09/25/2018
NUVASIVE, INC. NUVASIVE RELINE SYSTEM 08/21/2018
MEDTRONIC SOFAMOR DANEK ORTHOSIS, SPINAL PEDICLE FIXATION, FOR D 08/14/2018
NUVASIVE, INC. NUVASIVE RELINE SYSTEM 06/28/2018
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