Home GUDID 10888857008397 DENALI® Spinal System
Primary DI 10888857008397
Brand DENALI® Spinal System
Company K2M, INC.
Model 101-80041
Catalog number 101-80041
Device description Extended Body Hook, Standard, Size (S)
Published 2015-09-24
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name MNH Orthosis, spondylolisthesis spinal fixation
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10888857008397 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10888857008397 10888857008397
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An assembly of non-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. Non-sterile disposable devices associated with implantation may be included.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Outer Diameter 5.5 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 146060863 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# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 10888857596986 K2M General Instruments PRO-1002-03 PRO-1002-03 2026-03-24 10888857596993 K2M General Instruments PRO-1002-04 PRO-1002-04 2026-03-24 10888857580022 LITe® Pedicle Based Retractor PRO-1388-01 PRO-1388-01 2026-03-04 10888857580039 LITe® Pedicle Based Retractor PRO-1388-02 PRO-1388-02 2026-03-04 10888857580046 LITe® Pedicle Based Retractor PRO-1388-03 PRO-1388-03 2026-03-04 10888857580053 LITe® Pedicle Based Retractor PRO-1388-04 PRO-1388-04 2026-03-04 10888857580060 LITe® Pedicle Based Retractor PRO-1388-05 PRO-1388-05 2026-03-04 10888857580077 LITe® Pedicle Based Retractor PRO-1388-06 PRO-1388-06 2026-03-04 10888857580084 LITe® Pedicle Based Retractor PRO-1388-07 PRO-1388-07 2026-03-04 10888857563384 Q Interbody Instruments 8020-90020 8020-90020 2026-03-03 10888857563391 Q Interbody Instruments 8020-90021 8020-90021 2026-03-03 10888857563407 Q Interbody Instruments 8020-90022 8020-90022 2026-03-03 10888857563414 Q Interbody Instruments 8020-90023 8020-90023 2026-03-03 10888857563421 Q Interbody Instruments 8020-90024 8020-90024 2026-03-03 10888857563650 Q Interbody Instruments 8020-90086 8020-90086 2026-03-03 10888857574700 Q Interbody Instruments 8020-90092-GS 8020-90092-GS 2026-03-03 10888857578715 Q Interbody Instruments 8020-10001 8020-10001 2026-03-03 10888857578722 Q Interbody Instruments 8020-10002 8020-10002 2026-03-03 10888857578739 Q Interbody Instruments 8020-10003 8020-10003 2026-03-03 10888857578876 Q Interbody Instruments 8020-90025 8020-90025 2026-03-03
Other Devices Sharing Product Codes#