FDA UDI In Commercial Distribution 🇺🇸 United States

VIKOS Allograft System

DI: 10888857239531 · Model: 2504-90036 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VIKOS Allograft System
Primary DI
10888857239531
Version / Model
2504-90036
Catalog Number
2504-90036
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-23
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
9dcfab94-1036-42ec-b652-c9b204d0fdf0

Device Description

Trial Size 11.5x14.5x9 mm, 0°

Device Characteristics

Single Use
No
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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10888857239531

Customer Contacts