Vu LPOD™ 12-TA-3016

GUDID 10889981039196

Implant Tapered 30x16mm

SEASPINE ORTHOPEDICS CORPORATION

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 10889981039196
• NIH Device Record Key: 67de7a80-4891-447e-a3de-f73b650b74ad
• Commercial Distribution Discontinuation: 2016-09-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Vu LPOD™
• Version Model Number: 12-TA-3016
• Catalog Number: 12-TA-3016
• Company DUNS: 079840876
• Company Name: SEASPINE ORTHOPEDICS CORPORATION
• 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: false
• 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(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com
• Phone: +1(866)942-8698
• Email: custsvcspine@seaspine.com

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	10889981039196 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082712

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-24

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• 10889981333324 - Virata: 2025-10-06 Reducer Handle, Egg
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• 10889981336356 - Virata: 2025-10-06 Shank, CC, 6.0mm X 25mm