Home GUDID M711LS2740 Excella III-D®
Primary DI M711LS2740
Brand Excella III-D®
Company INNO Holdings, Inc.
Model LS-274
Catalog number LS-274
Device description Silicone, SST
Published 2019-07-05
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx 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 M711LS2740 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Orthopaedic rod reducer A heavy-duty, hand-held manual surgical instrument intended to be used to reduce or seat an implantable rod into the saddle of an implant (i.e., bone screw, spinal hook) used as a component of a system to apply force to a series of vertebrae to correct scoliosis (lateral curvature of the spine) or other spinal conditions. When the rod lies medial or lateral to the implant channel this instrument allows for controlled translation of the rod into the saddle of the screws and/or hooks. The surgeon is able to control the positioning (bending) of the rod into the saddle. Once the rod is securely seated in the saddle it is locked into position with a plug or a setscrew. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Lumen/Inner Diameter 5.5 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 141620464 Device count 1 Serial number true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840466901011 Primus SPINAL ELEMENTS, INC. KWP 2026-10-22 00840466901011 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840466901011 Primus SPINAL ELEMENTS, INC. KWQ 2026-10-22 00840606168472 SAPPHIRE X SPINAL ELEMENTS, INC. KWQ 2026-10-22 00840606168502 SAPPHIRE X SPINAL ELEMENTS, INC. KWQ 2026-10-22 00840606174855 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840606175142 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840606175203 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840606185868 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 03701313009823 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009830 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009854 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009878 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009885 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009892 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009908 KHEIRON S.M.A.I.O NKB 2026-10-22 00197157123611 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123628 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123635 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123642 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123659 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123666 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157122874 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122881 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122898 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122904 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122911 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122928 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122935 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122942 ZAVATION SCREW Zavation LLC NKB 2026-10-20