Idys™- LIF 06533314-S

GUDID 03700780604050

TLIF CAGE

CLARIANCE

Polymeric spinal interbody fusion cage

• Primary Device ID: 03700780604050
• NIH Device Record Key: 077290cd-87f0-44ae-8b03-2c4aa1b34073
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Idys™- LIF
• Version Model Number: 06533314-S
• Catalog Number: 06533314-S
• Company DUNS: 296568400
• Company Name: CLARIANCE
• 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: 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

Customer Support Contacts

• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us
• Phone: 7738687041
• Email: s.chambat@clariance-spine.us

Device Dimensions

• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter
• Height: 14 Millimeter
• Depth: 12 Millimeter
• Width: 33 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700780604050 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131178

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: 4
• Public Version Date: 2025-12-29
• Device Publish Date: 2015-10-23

On-Brand Devices [Idys™- LIF]

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• 03700780622481: PLIF CAGE
• 03700780604074: TLIF CAGE
• 03700780604067: TLIF CAGE
• 03700780604050: TLIF CAGE
• 03700780604043: TLIF CAGE
• 03700780604036: TLIF CAGE
• 03700780603787: TLIF CAGE
• 03700780603749: TLIF CAGE
• 03700780600465: TLIF CAGE
• 03700780600458: TLIF CAGE
• 03700780600441: TLIF CAGE
• 03700780600434: TLIF CAGE
• 03700780600427: TLIF CAGE
• 03700780600397: TLIF CAGE
• 03700780600373: PTLIF CAGE
• 03700780600366: PTLIF CAGE
• 03700780600359: PTLIF CAGE
• 03700780600342: PTLIF CAGE
• 03700780600335: PTLIF CAGE
• 03700780600311: PTLIF CAGE
• 03700780600298: PTLIF CAGE
• 03700780600281: PTLIF CAGE
• 03700780600274: PTLIF CAGE
• 03700780600267: PTLIF CAGE
• 03700780600243: PLIF CAGE
• 03700780600229: PLIF CAGE
• 03700780600212: PLIF CAGE
• 03700780600199: PLIF CAGE
• 03700780600182: PLIF CAGE
• 03700780600175: PLIF CAGE
• 03700780600168: PLIF CAGE
• 03700780600137: PLIF CAGE
• 03700780600120: PLIF CAGE