FDA UDI In Commercial Distribution 🇺🇸 United States

EVEREST® Spinal System

DI: 10888857104792 · Model: 5101-A60230 · VB Spine LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
EVEREST® Spinal System
Primary DI
10888857104792
Version / Model
5101-A60230
Catalog Number
5101-A60230
Company Name
VB Spine LLC
Labeler DUNS
119508156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-08
Public Version
5
Public Version Date
2026-04-20
Public Version Status
Update
Public Device Record Key
0ee15bbd-5d29-42aa-ac7c-52a06bfc585f

Device Description

Straight Rod, Bulleted Hex Size Ø6.0x230 mm, Ti

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

Code Name
65116 Bone-screw internal spinal fixation system rod

Identifiers

Type ID
Primary 10888857104792

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 6 Millimeter
Length 230 Millimeter