Veo Lateral Spinal System

GUDID 00840996177177

VEO Rasping Trail 17x9x6 deg

Choice Spine, LP

Polymeric spinal interbody fusion cage

• Primary Device ID: 00840996177177
• NIH Device Record Key: e0db1df1-7cbd-4fcf-8c4a-cc913600f763
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Veo Lateral Spinal System
• Version Model Number: V070-61709CG
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840996177177 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100210

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00840996177177]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-24
• Device Publish Date: 2019-06-20

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