Home GUDID 10888857089136 ALEUTIAN® Interbody Systems
Primary DI 10888857089136
Brand ALEUTIAN® Interbody Systems
Company K2M, INC.
Model 402-90234
Catalog number 402-90234
Device description Inserter, Size 20 mm
Published 2016-09-16
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 false Product Codes# Code, Name table Code Name MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MQP Spinal Vertebral Body Replacement Device Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10888857089136 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10888857089136 10888857089136
GMDN Terms# Term, Definition table Term Definition Orthopaedic prosthesis implantation instrument, reusable A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use.
Device Sizes# Type, Value, Unit table Type Value Unit Width 20 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# 
k2m.com
stryker.com