FDA UDI In Commercial Distribution 🇺🇸 United States

AXIOM®

DI: M68415780040001 · Model: 1578004000 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AXIOM®
Primary DI
M68415780040001
Version / Model
1578004000
Catalog Number
1578004000
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
3eb65709-ec15-4d83-a03d-6c78624b1574

Device Description

AXIOM® ADAPTIVE FIXATION SCREW 40mm AXIOM® FEM/PLUS TIB

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Direct Marking 1578004000
Primary M68415780040001

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K894334 000

Device Sizes

Type Value Unit Text
Length 40 Millimeter