186311513

GUDID 10705034118741

SURGICAL TITANIUM MESH TRAPEZOID MESH 11 x (13 x 15) x 20mm

DEPUY SPINE, LLC

Metallic spinal interbody fusion cage

• Primary Device ID: 10705034118741
• NIH Device Record Key: b1369247-74df-418a-ae0b-2882e7705277
• Commercial Distribution Discontinuation: 2018-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 186311513
• Catalog Number: 186311513
• Company DUNS: 107105876
• Company Name: DEPUY 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: 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034118741 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K030249

FDA Product Code

• MQP: SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Sterilization

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

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

[10705034118741]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2021-10-12
• Device Publish Date: 2015-09-24

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• 10705034584171 - TRIALTIS: 2025-07-25 ø5.5-6mm to 5.5-6mm
• 10705034587240 - TRIALTIS: 2025-07-25 ø5.5-6mm to 5.5-6mm
• 10705034587257 - TRIALTIS: 2025-07-25 ø5.5-6mm to 5.5-6mm
• 10705034587561 - TRIALTIS: 2025-07-25 ø5.5-6mm to 5.5mm x 40mm
• 10705034587578 - TRIALTIS: 2025-07-25 ø5.5-6mm to 5.5mm x 60mm
• 10705034587660 - TRIALTIS: 2025-07-25 ø5.5-6mm to 6mm x 20mm
• 10705034587684 - TRIALTIS: 2025-07-25 ø5.5-6mm to 6mm x 40mm