Home GUDID 10889981028534
Stainless Steel
Primary DI 10889981028534
Brand Stainless Steel
Company Seaspine Orthopedics Corporation
Model 25-22-3802
Catalog number 25-22-3802
Device description Adjustable Cross Connector, 38mm-40mm. The Stainless Steel Spinal System consists of a variety of types and sizes of rods, hooks, screws. The Stainless Steel Spinal System implant components can be rigidly locked into a variety of configurations that can be fit for the individual case. The Stainless Steel Spinal System uses components manufactured from 316 LVM stainless steel (ASTM F-138). Unless otherwise instructed, never use this product with components from another manufacturer or system.
Published 2015-09-24
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 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 10889981028534 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10889981028534 10889981028534
GMDN Terms# Term, Definition table Term Definition Vertebral body prosthesis, non-sterile A non-sterile implantable device designed to replace or repair (fuse) the spinal bony segments, or vertebrae, lost or injured as a consequence of, e.g., trauma, deformity, tumour, or degenerative disease. It is typically intended to be used with supplemental spinal fixation and may be used with a bone graft. It is usually made of metal, polymer, or a combination of these materials. This device must be sterilized prior to use.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 079840876 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 00763000859404 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. NKB 2026-07-18 00763000859404 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-18 00763000859404 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWQ 2026-07-18 00763000910365 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. NKB 2026-07-18 00763000910365 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWQ 2026-07-18 00763000910365 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-18 20763000910376 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-18 20763000910376 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. NKB 2026-07-18 20763000910376 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWQ 2026-07-18 18257200054206 SFS Orthofix US LLC NKB 2026-07-17 18257200054213 SFS Orthofix US LLC NKB 2026-07-17 18257200054220 SFS Orthofix US LLC NKB 2026-07-17 18257200054237 SFS Orthofix US LLC NKB 2026-07-17 18257200054244 SFS Orthofix US LLC NKB 2026-07-17 18257200054251 SFS Orthofix US LLC NKB 2026-07-17 18257200054268 SFS Orthofix US LLC NKB 2026-07-17 18257200054275 SFS Orthofix US LLC NKB 2026-07-17 18257200054282 SFS Orthofix US LLC NKB 2026-07-17 18257200054299 SFS Orthofix US LLC NKB 2026-07-17 18257200054305 SFS Orthofix US LLC NKB 2026-07-17 18257200054312 SFS Orthofix US LLC NKB 2026-07-17 00199150015832 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015849 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015856 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015863 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015870 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015887 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015894 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015900 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16 00199150015917 INFINITY™ Occipitocervical Upper Thoracic System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-07-16