Home GUDID 10889981049621 Integra Expandable Interbody
Primary DI 10889981049621
Brand Integra Expandable Interbody
Company Seaspine Orthopedics Corporation
Model 98-2921
Catalog number 98-2921
Device description 22mm Implant Caddy. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
Published 2015-09-24
Public version status Update
Distribution status Not in Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx 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 10889981049621 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10889981049621 10889981049621
GMDN Terms# Term, Definition table Term Definition Instrument tray A flat shallow vessel, usually with a raised rim, providing a suitable platform for containing many medical, usually surgical instruments and items. It is typically made of stainless steel and designed to fit into other devices, e.g., supply trolleys, storage systems and sterilizers; it is not dedicated to sterilization. This device may or may not be fitted with a lid or cover. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 079840876 Device count 1 Kit 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 00840606185110 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185127 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185134 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185141 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185158 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185165 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606196024 Vertu SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606196031 Vertu SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606196048 Vertu SPINAL ELEMENTS, INC. MAX 2026-09-25 00810017915170 SABER-XA, Screw Ø5.5 x 32.5 ELEVATION SPINE, INC. MAX 2026-09-22 10888857461819 CASCADIA™ Interbody System VB Spine LLC MAX 2019-10-31 10888857461888 CASCADIA™ Interbody System VB Spine LLC MAX 2019-10-31 04546540665720 AVS NAVIGATOR Stryker Corporation MAX 2016-09-24 10888857218772 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857218963 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857219076 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857219489 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857219595 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 07613153046196 AVS PL Stryker Corporation MAX 2015-09-14 07613153046202 AVS PL Stryker Corporation MAX 2015-09-14 07613153046219 AVS PL Stryker Corporation MAX 2015-09-14 07613153046226 AVS PL Stryker Corporation MAX 2015-09-14 07613153046233 AVS PL Stryker Corporation MAX 2015-09-14 07613153046288 AVS PL Stryker Corporation MAX 2015-09-14 07613153046295 AVS PL Stryker Corporation MAX 2015-09-14 07613153046301 AVS PL Stryker Corporation MAX 2015-09-14 07613153046318 AVS PL Stryker Corporation MAX 2015-09-14 07613153046325 AVS PL Stryker Corporation MAX 2015-09-14 07613153046332 AVS PL Stryker Corporation MAX 2015-09-14 07613153046349 AVS PL Stryker Corporation MAX 2015-09-14