FDA UDI In Commercial Distribution 🇺🇸 United States

VEO Lateral Interbody Fusion System

DI: 00840996148368 · Model: VT10-50220007 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VEO Lateral Interbody Fusion System
Primary DI
00840996148368
Version / Model
VT10-50220007
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-27
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
17a9887e-cef1-4ab4-a51c-0d9745b2c1b3

Device Description

LATERAL,SPACER 22,50X7.5,0 DEG

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
57805 Metallic spinal fusion cage, non-sterile

Identifiers

Type ID
Primary 00840996148368

Customer Contacts

Device Sizes

Type Value Unit Text
Length 50 Millimeter
Width 22 Millimeter
Height 7.5 Millimeter