ENDOSKELETON® TT nanoLOCK® Surface Technology

GUDID 00763000885748

NANO SPACER 4114-3508-N TT 4 DG XLG 8MM

MEDTRONIC SOFAMOR DANEK, INC.

Metallic spinal interbody fusion cage

• Primary Device ID: 00763000885748
• NIH Device Record Key: 71855056-3bd6-425f-94a4-5c533862ca94
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDOSKELETON® TT nanoLOCK® Surface Technology
• Version Model Number: 4114-3508-N
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, 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(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000885748 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141953

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: 2025-06-30
• Device Publish Date: 2025-06-22

On-Brand Devices [ENDOSKELETON® TT nanoLOCK® Surface Technology]

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• 00763000885786: NANO SPACER 4114-3512-N TT 4 DG XLG 12MM
• 00763000885762: NANO SPACER 4114-3510-N TT 4 DG XLG 10MM
• 00763000885748: NANO SPACER 4114-3508-N TT 4 DG XLG 8MM
• 00763000885731: NANO SPACER 4114-3014-N TT 4 DG LG 14MM
• 00763000885724: NANO SPACER 4114-3013-N TT 4 DG LG 13MM
• 00763000885694: NANO SPACER 4114-3010-N TT 4 DG LG 10MM
• 00763000885687: NANO SPACER 4114-3009-N TT 4 DG LG 9MM
• 00763000885670: NANO SPACER 4114-3008-N TT 4 DG LG 8MM
• 00763000885779: NANO SPACER 4114-3511-N TT 4 DG XLG 11MM