FortiCore® 11302-3408

GUDID 00814216020864

FortiCore® TLIF Spacer 8x13x34, (6°)

NANOVIS SPINE, LLC

Metal-polymer composite spinal interbody fusion cage

• Primary Device ID: 00814216020864
• NIH Device Record Key: 7fb068bd-8846-4d2f-a23e-682a1d75b8a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FortiCore®
• Version Model Number: 11302-3408
• Catalog Number: 11302-3408
• Company DUNS: 079898044
• Company Name: NANOVIS SPINE, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 8779076266
• Email: nanovisquality@nanovistechnology.com
• Phone: 8779076266
• Email: nanovisquality@nanovistechnology.com

Device Dimensions

• Width: 13 Millimeter
• Width: 13 Millimeter
• Width: 13 Millimeter
• Width: 13 Millimeter
• Width: 13 Millimeter
• Width: 13 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814216020864 [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: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-02-24
• Device Publish Date: 2015-09-15

On-Brand Devices [FortiCore® ]

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