Home GUDID 00193082167300
ORIO-3D Cage System
Primary DI 00193082167300
Brand ORIO-3D Cage System
Company SPINECRAFT, LLC
Model SP-LP-ST12-1126
Catalog number SP-LP-ST12-1126
Device description ORIO-3D Trabecular Ti TLIF Cage, Straight, 10mm Wide, 11 x 26mm, 12 deg.
Published 2026-05-20
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true
Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar ODP Intervertebral fusion device with bone graft, cervical OVD Intervertebral fusion device with integrated fixation, lumbar
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2 ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic 2 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00193082167300 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00193082167300 00193082167300 193082167300 0193082167300
GMDN Terms# Term, Definition table Term Definition Metallic spinal interbody fusion cage A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated cylindrical, or disc-shaped device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.
Regulatory Flags# DUNS number 783908713 Device count 1 DM exempt true Lot or batch true Expiration date on label true No natural rubber latex true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00193082162084 ANTERIS Thoracolumbar Plate System LPS-APSD-10 LPS-APSD-10 2026-05-20 00193082162091 ANTERIS Thoracolumbar Plate System LPS-APSD-12 LPS-APSD-12 2026-05-20 00193082162107 ANTERIS Thoracolumbar Plate System LPS-APSD-14 LPS-APSD-14 2026-05-20 00193082162114 ANTERIS Thoracolumbar Plate System LPS-APSD-16 LPS-APSD-16 2026-05-20 00193082162121 ANTERIS Thoracolumbar Plate System LPS-APSD-18 LPS-APSD-18 2026-05-20 00193082162138 ANTERIS Thoracolumbar Plate System LPS-APSD-20 LPS-APSD-20 2026-05-20 00193082162145 ANTERIS Thoracolumbar Plate System LPS-APSD-22 LPS-APSD-22 2026-05-20 00193082162152 ANTERIS Thoracolumbar Plate System LPS-APSD-24 LPS-APSD-24 2026-05-20 00193082162169 ANTERIS Thoracolumbar Plate System LPS-APSL-10 LPS-APSL-10 2026-05-20 00193082162176 ANTERIS Thoracolumbar Plate System LPS-APSL-12 LPS-APSL-12 2026-05-20 00193082162183 ANTERIS Thoracolumbar Plate System LPS-APSL-14 LPS-APSL-14 2026-05-20 00193082162190 ANTERIS Thoracolumbar Plate System LPS-APSL-16 LPS-APSL-16 2026-05-20 00193082162206 ANTERIS Thoracolumbar Plate System LPS-APSL-18 LPS-APSL-18 2026-05-20 00193082162213 ANTERIS Thoracolumbar Plate System LPS-APSL-20 LPS-APSL-20 2026-05-20 00193082162220 ANTERIS Thoracolumbar Plate System LPS-APSL-22 LPS-APSL-22 2026-05-20 00193082162237 ANTERIS Thoracolumbar Plate System LPS-APSL-24 LPS-APSL-24 2026-05-20 00193082162688 ANTERIS Thoracolumbar Plate System LPS-APS50-30 LPS-APS50-30 2026-05-20 00193082162695 ANTERIS Thoracolumbar Plate System LPS-APS55-30 LPS-APS55-30 2026-05-20 00193082162701 ANTERIS Thoracolumbar Plate System LPS-APS50-20 LPS-APS50-20 2026-05-20 00193082162718 ANTERIS Thoracolumbar Plate System LPS-APS55-20 LPS-APS55-20 2026-05-20
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