FDA UDI In Commercial Distribution 🇺🇸 United States

Fuji Cervical Plate System

DI: B41711140221 · Model: 111-4022 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Fuji Cervical Plate System
Primary DI
B41711140221
Version / Model
111-4022
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-22
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
1e2d702b-c3fc-41c4-a839-b04f290036ab

Device Description

4.0mm Variable Angle Self Drilling

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
Yes
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

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary B41711140221
Secondary 00843210102672

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K163061 000

Device Sizes

Type Value Unit Text
Length 22 Millimeter
Outer Diameter 4 Millimeter