TILT®

GUDID 00190361002185

TILT IBC, 9mm Straight, 38x12

SPINEFRONTIER, INC.

Polymeric spinal interbody fusion cage

• Primary Device ID: 00190361002185
• NIH Device Record Key: 7e12998d-8529-4655-bc12-e38bfedf3e35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TILT®
• Version Model Number: 01-04022-3812
• Company DUNS: 002003243
• Company Name: SPINEFRONTIER, INC.
• Device Count: 1
• DM Exempt: true
• 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(866)914-7717
• Email: customerservice@spinefrontier.com

Device Dimensions

• Width: 9 Millimeter
• Width: 9 Millimeter
• Width: 9 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190361002185 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111553

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[00190361002185]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2016-04-15

On-Brand Devices [TILT®]

• 00190361002208: TILT IBC, 9mm Straight, 38x14
• 00190361002192: TILT IBC, 9mm Straight, 38x13
• 00190361002185: TILT IBC, 9mm Straight, 38x12
• 00190361002178: TILT IBC, 9mm Straight, 38x11
• 00190361002161: TILT IBC, 9mm Straight, 38x10
• 00190361002154: TILT IBC, 9mm Straight, 38x9
• 00190361002147: TILT IBC, 9mm Straight, 38x8