Home GUDID B030ORO85110R0 ORTHROS
Primary DI B030ORO85110R0
Brand ORTHROS
Company CAMBER SPINE TECHNOLOGIES, LLC
Model ORO-85110R
Device description Ø8.5mm polyaxial reduction pedicle screw , 110mm lg.
Published 2016-11-03
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 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 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 B030ORO85110R0 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Polymeric 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 in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] 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 included with the device.
Device Sizes# Type, Value, Unit table Type Value Unit Length 110 Millimeter Outer Diameter 8.5 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 054205979 Device count 1 Lot or batch true Manufacturing date on label true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published B030SPO1530020 VARIANT SPO-153-002 2022-11-25 B030TLP420WR0 Alcantara™ Thoracolumbar Plating TLP-420WR 2025-08-01 B030TLP422WR0 Alcantara™ Thoracolumbar Plating TLP-422WR 2025-08-01 B030TLP424WR0 Alcantara™ Thoracolumbar Plating TLP-424WR 2025-08-01 B030TLP426WR0 Alcantara™ Thoracolumbar Plating TLP-426WR 2025-08-01 B030TLP428WR0 Alcantara™ Thoracolumbar Plating TLP-428WR 2025-08-01 B030TLP430WR0 Alcantara™ Thoracolumbar Plating TLP-430WR 2025-08-01 B030TLP432WR0 Alcantara™ Thoracolumbar Plating TLP-432WR 2025-08-01 B030TLP434WR0 Alcantara™ Thoracolumbar Plating TLP-434WR 2025-08-01 B030TLP436WR0 Alcantara™ Thoracolumbar Plating TLP-436WR 2025-08-01 B030TLP438WR0 Alcantara™ Thoracolumbar Plating TLP-438WR 2025-08-01 B030TLP440WR0 Alcantara™ Thoracolumbar Plating TLP-440WR 2025-08-01 B030TLP1000 Alcantara Thoracolumbar Plating TLP-100 NA 2024-07-18 B030TLP2180 Alcantara Thoracolumbar Plating TLP-218 NA 2024-07-18 B030TLP2200 Alcantara Thoracolumbar Plating TLP-220 NA 2024-07-18 B030TLP2220 Alcantara Thoracolumbar Plating TLP-222 NA 2024-07-18 B030TLP2240 Alcantara Thoracolumbar Plating TLP-224 NA 2024-07-18 B030TLP2260 Alcantara Thoracolumbar Plating TLP-226 NA 2024-07-18 B030TLP2280 Alcantara Thoracolumbar Plating TLP-228 NA 2024-07-18 B030TLP2350 Alcantara Thoracolumbar Plating TLP-235 NA 2024-07-18
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