Home GUDID 00190376396804 Calibrate
Primary DI 00190376396804
Brand Calibrate
Company ALPHATEC SPINE, INC.
Model 320-08142500
Device description PSX Lordotic Expandable, 8 x 14 x 25mm, 20°
Published 2022-01-22
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true
Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00190376396804 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 00190376396804 00190376396804 190376396804 0190376396804
GMDN Terms# Term, Definition table Term Definition Metallic spinal interbody fusion cage A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
Device Sizes# Type, Value, Unit table Type Value Unit Angle 20 degree Height 8 Millimeter Length 25 Millimeter Width 14 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 602465783 Device count 1 DM exempt true 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 00843511102852 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102869 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102876 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102883 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102890 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102906 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102913 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102920 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00193982141097 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141103 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141110 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141127 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141134 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141141 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141158 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141165 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141172 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141189 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141196 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141202 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141240 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141257 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141264 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141271 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141288 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141295 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141301 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141318 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141325 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141332 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14