Veo Lateral Spinal System

GUDID 00840996176422

VEO, Ring Shavers

Choice Spine, LP

Polymeric spinal interbody fusion cage

• Primary Device ID: 00840996176422
• NIH Device Record Key: 288754b3-255e-48da-8b6e-60863c7f137c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Veo Lateral Spinal System
• Version Model Number: V070-0092
• Company DUNS: 078293017
• Company Name: Choice Spine, LP
• 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: 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(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM
• Phone: +1(865)246-3333
• Email: INFO@CHOICESPINE.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840996176422 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123997

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

[00840996176422]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-24
• Device Publish Date: 2022-11-16

On-Brand Devices [Veo Lateral Spinal System]

• 00840996177207: VEO Rasping Trail 17x15x6 deg
• 00840996177191: VEO Rasping Trail 17x13x6 deg
• 00840996177184: VEO Rasping Trail 17x11x6 deg
• 00840996177177: VEO Rasping Trail 17x9x6 deg
• 00840996177160: VEO Rasping Trail 17x8x6 deg
• 00840996176422: VEO, Ring Shavers
• 00840996176415: VEO, Ring Shavers
• 00840996176408: VEO, Ring Shavers