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    NQO

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·April 11, 2011

    NQO

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·April 11, 2011

    NQO

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·April 11, 2011

    Superion Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm

    FDA Recall
    Open, Classified ·Boston Scientific Neuromodulation Corporation·Product code NQO·October 12, 2022

    Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect Decompression System IFU, Superion IDS Kit IFU, Surgical Technique Manual

    FDA Recall
    Open, Classified ·Boston Scientific Neuromodulation Corporation·Product code NQO·May 12, 2023

    St. Francis Medical Technologies brand X STOP Interspinous Process Decompression (IPD) System, 14 mm X STOP implants in peel pouch, Catalog #1-2210; The X STOP consists of a main body, a spacer, and a tissue expander that is secured using a universal wing assembly consisting of a wing and a setscrew. Product is distributed by St. Francis Medical Technologies, Inc., 960 Atlantic Avenue, Suite 102, Alameda, CA 94501

    FDA Recall
    Terminated ·St. Francis Medical Technologies Inc·Product code NQO·June 6, 2006

    X-STOP Interspinous Process Decompression (lPD) System, (With Physician's Guide, P/N 16000789-01 (Ti device), P/N 16001013-01 (PEEK device); Catalog numbers for X-STOP Titanium Implant: 1-2206 US 6MM X-STOP, 1-2208 US 8MM X-STOP, 1-2210 US 10MM X-STOP, 1-2212 US 12MM X-STOP, 1-2214 US 14MM X-STOP. Catalog numbers include for X-STOP PEEK Implant: 1-3206 US 6mm X STOPpk, 1-3208 US 8mm X STOPpk, 1-3210 US 10mm X STOPpk, 1-3212 US 12mm X STOPpk, 1-3214 US 14mm X STOPpk, 1-3216 US 16mm X STOPpk. Product is manufactured and distributed by Medtronic Spine LLC (formerly Kyphon Inc.); Spinal implants.

    FDA Recall
    Terminated ·Kyphon Inc·Product code NQO·January 30, 2008

    Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect Decompression System 10MM, VF Implant 101-9810 00884662000536 Superion Indirect Decompression System 12MM, VF Implant 101-9812 00884662000543 Superion Indirect Decompression System 14MM, VF Implant 101-9814 00884662000550 Superion Indirect Decompression System 16MM, VF Implant 101-9816 00884662000567 Superion Indirect Decompression System Kit, VF Instrument 102-9800 00884662000574 The Vertiflex Procedure Instrument Platform, VF Instrument 140-9800 00884662000611 The Superion IDS Kit includes a set of proprietary instruments to deliver the Superion Implant in a minimally invasive manner. Instruments specifically designed for implanting the Superion Implant are sterile, single-use disposable instruments, consisting of a Dilator Assembly, Cannula Assembly, Interspinous Gauge, Inserter, Reamer, and Driver.

    FDA Recall
    Open, Classified ·Boston Scientific Neuromodulation Corporation·Product code NQO·June 6, 2025

    Spacers of varying lengths used with the InSTANT Stranding System, Part numbers: TG3138, TG3139, TG3140, TG3141 and TG3142. Theragenics Corporation, 5203 Bristol Industrial Way, Buford GA 30518. The spacer product is intended for consumption during the brachytherapy procedure. Unused (unopened) product is not intended to be inventoried. by the attending physician.

    FDA Recall
    Terminated ·Theragenics Corporation·Product code NQO·December 8, 2008

    PROSTHESIS, SPINOUS PROCESS SPACER/PLATE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQO·December 22, 2016

    PROSTHESIS, SPINOUS PROCESS SPACER/PLATE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQO·December 23, 2016

    PROSTHESIS, SPINOUS PROCESS SPACER/PLATE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code NQO·December 23, 2016

    COFLEX INTERLAMINAR TECHNOLOGY

    FDA Adverse Event
    Injury ·PARADIGM SPINE GMBH·Product code NQO·December 19, 2016

    X-STOP PEEK INTERSPINOUS SPACER

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NQO·September 16, 2015

    X-STOP®PEEK INTERSPINOUS SPACER

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQO·July 7, 2015

    X-STOP INTERSPINOUS SPACER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQO·September 23, 2015

    PROSTHESIS, SPINOUS PROCESS SPACER/PLATE

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·March 9, 2012

    X-STOP INTERSPINOUS SPACER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·February 1, 2012

    X-STOP INTERSPINOUS SPACER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·February 1, 2012

    PROSTHESIS, SPINOUS PROCESS SPACER/PLATE

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·March 13, 2012