TALOS®-T 2-21109-00

GUDID 07640332475898

TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L28 W10 H09

SpineArt SA

Polymeric spinal interbody fusion cage

• Primary Device ID: 07640332475898
• NIH Device Record Key: a56d7f52-2b96-48d5-960d-431ac603ae0c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TALOS®-T
• Version Model Number: 2-21109-00
• Catalog Number: 2-21109-00
• Company DUNS: 483016148
• Company Name: SpineArt SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640332475898 [Primary]

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-11-28
• Device Publish Date: 2025-11-20

On-Brand Devices [TALOS®-T]

• 07640332476048: TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L32 W10 H14
• 07640332475911: TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L28 W10 H11
• 07640332475904: TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L28 W10 H11
• 07640332475898: TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L28 W10 H09
• 07640332475881: TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L28 W10 H08
• 07640332475874: TALOS-T (HA) LORDOTIC HA PEEK IBFD 0° L28 W10 H07