176302010

GUDID 10705034036984

SURGICAL TITANIUM MESH MESH LT 23X27 OVAL TRAPEZOID 10 x 12mm

DEPUY SPINE, LLC

Metallic spinal interbody fusion cage

• Primary Device ID: 10705034036984
• NIH Device Record Key: ee8a3365-d001-4031-bae7-5b1611a63b13
• Commercial Distribution Discontinuation: 2018-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 176302010
• Catalog Number: 176302010
• 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	10705034036984 [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

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

Moist Heat or Steam Sterilization

[10705034036984]

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

Devices Manufactured by DEPUY SPINE, LLC

• 10705034577319 - N/A: 2025-04-11 TAP 4.0mm
• 10705034577326 - N/A: 2025-04-11 TAP 4.5mm
• 10705034577333 - N/A: 2025-04-11 TAP 5.0mm
• 10705034577340 - N/A: 2025-04-11 TAP 6.0mm
• 10705034577357 - N/A: 2025-04-11 TAP 7.0mm
• 10705034577647 - N/A: 2025-04-11 DRIVER T27
• 10705034577661 - N/A: 2025-04-11 DISTRACTOR
• 10705034577784 - N/A: 2025-04-11 DILATOR