FDA UDI In Commercial Distribution 🇺🇸 United States

MOJAVE Expandable Interbody System

DI: 10888857343733 · Model: 7012-2112408C-G2 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MOJAVE Expandable Interbody System
Primary DI
10888857343733
Version / Model
7012-2112408C-G2
Catalog Number
7012-2112408C-G2
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-19
Public Version
5
Public Version Date
2023-09-14
Public Version Status
Update
Public Device Record Key
01cbf444-58b4-4623-9d24-2a8204dfb895

Device Description

Expandable Interbody, Size 11x24x8-11 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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 10888857343733

Customer Contacts

Device Sizes

Type Value Unit Text
Length 24 Millimeter
Height 8 Millimeter
Device Size Text, specify Convex
Width 11 Millimeter
Device Size Text, specify 8-11 mm