Home GUDID 00889929026793
Inertia® Pedicle Screw and Deformity Correxxion® System
Primary DI 00889929026793
Brand Inertia® Pedicle Screw and Deformity Correxxion® System
Company NEXXT SPINE, LLC
Model 10-4-003
Device description Set Screw, 95105
Published 2018-08-22
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Single use true
Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal MNH Orthosis, Spondylolisthesis Spinal Fixation MNI Orthosis, Spinal Pedicle Fixation NKB Thoracolumbosacral Pedicle Screw System OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2 NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2 OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00889929026793 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 00889929026793 00889929026793 889929026793 0889929026793
GMDN Terms# Term, Definition table Term Definition Spinal bone set screw A small, threaded, implantable, non-bioabsorbable disc intended to be threaded into the proximal end of a spinal bone screw (screw head), anchor, connector and/or hook (none included) to secure/stabilize a rod and/or tether as part of an internal spinal fixation procedure or a treatment for idiopathic scoliosis. It is made of metal (e.g., surgical steel, titanium alloy).
Device Sizes# Type, Value, Unit table Type Value Unit Length 4.5 Millimeter Outer Diameter 12 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 003489810 Device count 1 Lot or batch 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 B678520297S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520297S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520297S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10