Alamo C Interbody Fusion Device 1412I-711

GUDID M6861412I7110

Cervical Interbody Fusion Device, PEEK

ALLIANCE PARTNERS LLC

Polymeric spinal interbody fusion cage

• Primary Device ID: M6861412I7110
• NIH Device Record Key: f31828d5-c5eb-4e37-a15d-6043c92b26bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alamo C Interbody Fusion Device
• Version Model Number: 1412I-711
• Catalog Number: 1412I-711
• Company DUNS: 962768169
• Company Name: ALLIANCE PARTNERS 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: false
• 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: +1(210)314-2525
• Email: info@alliance-spine.com

Device Dimensions

• Width: 14 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M6861412I7110 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112361

FDA Product Code

• ODP: Intervertebral fusion device with bone graft, cervical

Sterilization

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

[M6861412I7110]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-02-24
• Device Publish Date: 2017-10-03

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