176213020

GUDID 10705034036809

SURGICAL TITANIUM MESH MESH, 13 x 17mm OBLONG 20mm

DEPUY SPINE, LLC

Metallic spinal fusion cage, non-sterile

• Primary Device ID: 10705034036809
• NIH Device Record Key: 36648cff-ed5d-41a9-a368-222cc68087f8
• Commercial Distribution Discontinuation: 2019-04-30
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 176213020
• Catalog Number: 176213020
• 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
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034036809 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K900138

FDA Product Code

• EZX: Mesh, surgical, metal

Sterilization

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

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

[10705034036809]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-04-30
• Device Publish Date: 2015-09-24

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• 10705034577395 - N/A: 2025-05-07 ALIGNMENT GUIDE, FAS
• 10705034577401 - N/A: 2025-05-07 ALIGNMENT GUIDE, STANDARD
• 10705034577418 - N/A: 2025-05-07 DOUBLE ENDED PROBE