FDA UDI In Commercial Distribution 🇺🇸 United States

ADVANCE®

DI: M68475520040001 · Model: 7552004000 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ADVANCE®
Primary DI
M68475520040001
Version / Model
7552004000
Catalog Number
7552004000
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-23
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
d3e80cf6-1349-45c8-ba46-5f9dc5cda3dc

Device Description

CANCELLOUS BONE SCREW 6.5mm X 40mm

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
MR Conditional
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 7552004000
Primary M68475520040001

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K894334 000

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Outer Diameter 6.5 Millimeter