Home GUDID 00643169502017
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
Primary DI 00643169502017
Brand DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
Company MEDTRONIC SOFAMOR DANEK, INC.
Model 2154120
Device description INTERBODY 2154120 SMALL - 24 DEG 20MM
Published 2016-04-09
Public version status Update
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 KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY MAX Intervertebral fusion device with bone graft, lumbar OVD Intervertebral fusion device with integrated fixation, lumbar
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWQ Appliance, Fixation, Spinal Intervertebral Body Orthopedic 2 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 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 00643169502017 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 00643169502017 00643169502017 643169502017 0643169502017
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, sterile An assembly of sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Sterile disposable devices associated with implantation may be included.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Regulatory Flags# DUNS number 830350380 Device count 1 Lot or batch true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00199150002139 N/A 59325013 2026-07-16 00199150002146 N/A 59325016 2026-07-16 00199150015832 INFINITY™ Occipitocervical Upper Thoracic System 36537025 2026-07-16 00199150015849 INFINITY™ Occipitocervical Upper Thoracic System 36537030 2026-07-16 00199150015856 INFINITY™ Occipitocervical Upper Thoracic System 36537035 2026-07-16 00199150015863 INFINITY™ Occipitocervical Upper Thoracic System 36537040 2026-07-16 00199150015870 INFINITY™ Occipitocervical Upper Thoracic System 36537045 2026-07-16 00199150015887 INFINITY™ Occipitocervical Upper Thoracic System 36537050 2026-07-16 00199150015894 INFINITY™ Occipitocervical Upper Thoracic System 36537055 2026-07-16 00199150015900 INFINITY™ Occipitocervical Upper Thoracic System 36537060 2026-07-16 00199150015917 INFINITY™ Occipitocervical Upper Thoracic System 36537065 2026-07-16 00199150015924 INFINITY™ Occipitocervical Upper Thoracic System 36537070 2026-07-16 00199150015931 INFINITY™ Occipitocervical Upper Thoracic System 36537075 2026-07-16 00199150015948 INFINITY™ Occipitocervical Upper Thoracic System 36537080 2026-07-16 00199150015955 INFINITY™ Occipitocervical Upper Thoracic System 36537085 2026-07-16 00199150015962 INFINITY™ Occipitocervical Upper Thoracic System 36537090 2026-07-16 00199150015986 INFINITY™ Occipitocervical Upper Thoracic System 36537100 2026-07-16 00199150016006 INFINITY™ Occipitocervical Upper Thoracic System 36537110 2026-07-16 00199150016013 INFINITY™ Occipitocervical Upper Thoracic System 36537120 2026-07-16 00199150016037 INFINITY™ Occipitocervical Upper Thoracic System 36535060 2026-07-16
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