FDA UDI In Commercial Distribution 🇺🇸 United States

EVEREST® Spinal System

DI: 10888857324879 · Model: ME5112-01040 · K2M, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVEREST® Spinal System
Primary DI
10888857324879
Version / Model
ME5112-01040
Catalog Number
ME5112-01040
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
5
Public Version Date
2023-09-06
Public Version Status
Update
Public Device Record Key
7f7a1d93-3819-46eb-986b-d43e7870fb5e

Device Description

Sacroiliac Screw Extended Tab Cannulated, Size Dia. 10.5x40 mm

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
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
MNH Orthosis, spondylolisthesis spinal fixation
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10888857324879

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 10.5 Millimeter
Length 40 Millimeter