VEO® Lateral Interbody Fusion System

GUDID 00840996119863

LATERAL,SPACER 17,65X9,0 DEG

Choice Spine, LP

Polymeric spinal interbody fusion cage

• Primary Device ID: 00840996119863
• NIH Device Record Key: 851c1559-eef9-4ea7-9c0a-624760373c50
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VEO® Lateral Interbody Fusion System
• Version Model Number: 22-0467-06
• Company DUNS: 078293017
• Company Name: Choice Spine, LP
• 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(865)246-3333
• Email: info@choicespine.net

Device Dimensions

• Width: 17 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840996119863 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123997

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[00840996119863]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2015-10-24

On-Brand Devices [VEO® Lateral Interbody Fusion System]

• 00840996174688: VEO,DISTRACTOR,PADDLE,17X0 DEG,5H
• 00840996174671: VEO,DISTRACTOR,PADDLE,22X0 DEG,4H
• 00840996174664: VEO,DISTRACTOR,PADDLE,17X0 DEG,4H
• 00840996173230: VEO,DISTRACTOR,PADDLE,22X0 DEG
• 00840996173223: VEO,DISTRACTOR,PADDLE,17X0 DEG
• 00840996148092: SPCL,LATERAL,RAKE,ANGLED,10MM
• 00840996148085: SPCL,LATERAL,RAKE,10MM
• 00840996148078: SPCL,LATERAL, RASP, SINGLED SIDED
• 00840996148061: SPCL,VEO,RING SHAVER,14
• 00840996148054: SPCL,VEO,RING SHAVER,12
• 00840996148047: SPCL,VEO,RING SHAVER,10
• 00840996148030: SPCL,VEO,RING SHAVER,8
• 00840996148023: SPCL,VEO,CUP SHAVER
• 00840996146197: VEO,INNER SLEEVE
• 00840996135900: LATERAL,PADDLE SHAVER,15
• 00840996135894: LATERAL,PADDLE SHAVER,14
• 00840996135887: LATERAL,PADDLE SHAVER,13
• 00840996135870: LATERAL,PADDLE SHAVER,12
• 00840996135863: LATERAL,PADDLE SHAVER,11
• 00840996135856: LATERAL,PADDLE SHAVER,10
• 00840996135849: LATERAL,PADDLE SHAVER,9
• 00840996135832: LATERAL,PADDLE SHAVER,8
• 00840996135825: LATERAL,PADDLE SHAVER,7
• 00840996135061: LATERAL,COBB ELEVATOR,15 DEG
• 00840996135054: LATERAL,6MM FERRIS SMITH
• 00840996135047: LATERAL,4MM FERRIS SMITH
• 00840996135030: LATERAL,SLOTTED CIRC. SECONDARY
• 00840996135023: LATERAL,OBLONG RETRACTOR
• 00840996135016: LATERAL,UNILATERAL C-SECONDARY
• 00840996135009: LATERAL,17MM VEO IMPLANT
• 00840996134996: LATERAL,VEO MALLEABLE RETRACTOR
• 00840996134989: LATERAL,TRIAL HANDLE,SLIM
• 00840996134972: LATERAL,CYLINDRICAL STADIUM
• 00840996134965: LATERAL,5MM TOOTHED PITUITARY
• 00840996134958: LATERAL,BLUNT LATERAL ACCESS
• 00840996134941: LATERAL, STRAIGHT, ENDPLATE, RASP
• 00840996134934: LATERAL,LIGHT,STADIUM
• 00840996134927: LATERAL,DILATOR
• 00840996134910: LATERAL,RETRACTOR
• 00840996134903: LATERAL,TWO LEVEL,25-9029
• 00840996134897: LATERAL,SINGLE LEVEL WITH PROBE
• 00840996134880: LATERAL,SINGLE LEVEL
• 00840996134873: LATERAL,MUSCLE RETRACTOR,200
• 00840996134866: LATERAL,MUSCLE RETRACTOR,180
• 00840996134859: LATERAL,NERVE RETRACTOR
• 00840996134842: LATERAL,SPACER INSERTER,ANGLED,LEFT,UP
• 00840996134835: LATERAL,COBB ELEVATOR 16,ANGLED,DOWN
• 00840996134828: LATERAL,COBB ELEVATOR 16,ANGLED,UP
• 00840996134811: LATERAL,12MM COBB DISSECTOR
• 00840996134804: LATERAL,LARGE LATERAL REVERSE