Home GUDID M711LS1490 Excella II®
Primary DI M711LS1490
Brand Excella II®
Company INNO Holdings, Inc.
Model LS-149
Catalog number LS-149
Device description SST
Published 2018-01-31
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal KWQ Appliance, Fixation, Spinal Intervertebral Body MNH Orthosis, Spondylolisthesis Spinal Fixation MNI Orthosis, Spinal Pedicle Fixation NKB Thoracolumbosacral Pedicle Screw System
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 KWQ Appliance, Fixation, Spinal Intervertebral Body Orthopedic 2 MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2 NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status M711LS1490 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Orthopaedic bone wire A wire intended for the fixation of bone fractures that may be implanted or used short-term (e.g., to hold a plate in the correct position during an intervention). It may be used: 1) as a cerclage wire to aid bone fixation; 2) in a loop or figure-of-eight configuration to reattach, e.g., the tip of the elbow (olecranon), tibial tubercle, or greater trochanter; 3) to augment bone screw/plate fixation; or 4) as a Kirschner wire or K-Wire to stiffen (arthrodese) a toe or finger. It is made of metal [e.g., stainless steel, cobalt-chrome (Co-Cr)], and may be malleable or rigid; some types include a nut designed to be attached to the wire to prevent wire migration. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Outer Diameter 1.5 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 141620464 Device count 1 DM exempt true Lot or batch true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published M711BTA2020 Vector™ Pedicle Screw System BTA-202 2026-06-05 M711LS7490 Vector™ Pedicle Screw System LS-749 2026-06-05 M711511410070 Endeavor™ Stand-Alone Cervical 51-141007 2026-05-31 M711511410120 Endeavor™ Stand-Alone Cervical 51-141012 2026-05-31 M711511411070 Endeavor™ Stand-Alone Cervical 51-141107 2026-05-31 M711511411120 Endeavor™ Stand-Alone Cervical 51-141112 2026-05-31 M711511412070 Endeavor™ Stand-Alone Cervical 51-141207 2026-05-31 M711511412120 Endeavor™ Stand-Alone Cervical 51-141212 2026-05-31 M711511606070 Endeavor™ Stand-Alone Cervical 51-160607 2026-05-31 M711511607070 Endeavor™ Stand-Alone Cervical 51-160707 2026-05-31 M711511607120 Endeavor™ Stand-Alone Cervical 51-160712 2026-05-31 M711511608070 Endeavor™ Stand-Alone Cervical 51-160807 2026-05-31 M711511608120 Endeavor™ Stand-Alone Cervical 51-160812 2026-05-31 M711511609070 Endeavor™ Stand-Alone Cervical 51-160907 2026-05-31 M711511609120 Endeavor™ Stand-Alone Cervical 51-160912 2026-05-31 M711511610070 Endeavor™ Stand-Alone Cervical 51-161007 2026-05-31 M711511610120 Endeavor™ Stand-Alone Cervical 51-161012 2026-05-31 M711511611070 Endeavor™ Stand-Alone Cervical 51-161107 2026-05-31 M711511611120 Endeavor™ Stand-Alone Cervical 51-161112 2026-05-31 M711511612070 Endeavor™ Stand-Alone Cervical 51-161207 2026-05-31
Other Devices Sharing Product Codes# 
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