Home GUDID M711E3S65400
Excella III-D®
Primary DI M711E3S65400
Brand Excella III-D®
Company INNO Holdings, Inc.
Model E3S6540
Catalog number E3S6540
Device description Ti 6Al 4V (ELI)
Published 2014-09-16
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 Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
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 M711E3S65400 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Spinal bone screw, non-bioabsorbable A small, threaded, implantable rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.
Device Sizes# Type, Value, Unit table Type Value Unit Length 40 Millimeter Outer Diameter 6.5 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# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 07290115935578 PER Trial 60 PREMIA SPINE LTD NKB 2026-07-22 07290115935691 PER Trial 50 PREMIA SPINE LTD NKB 2026-07-22 00840466901035 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901035 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901035 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901042 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901042 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901042 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901059 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901059 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901059 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901066 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901066 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901066 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901073 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901073 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901073 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901080 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901080 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901080 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901097 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901097 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901097 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901103 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901103 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901103 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901110 Primus SPINAL ELEMENTS, INC. NKB 2026-07-21 00840466901110 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901110 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901127 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21