Home GUDID 00887517156822
ReLine
Primary DI 00887517156822
Brand ReLine
Company Nuvasive, Inc.
Model 11010530
Catalog number 11010530
Device description GSB Screw, 10.5x30 mm 2S Polyaxial
Published 2026-04-25
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
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 Thoracolumbosacral pedicle screw system
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 00887517156822 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 00887517156822 00887517156822 887517156822 0887517156822
GMDN Terms# Term, Definition table Term Definition Spinal bone screw, non-bioabsorbable A small, threaded, implantable rod with a screw head and drive intended 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 (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 053950783 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false 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. NKB 2026-07-18 20763000910376 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWQ 2026-07-18 20763000910376 CD Horizon™ Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWP 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