FDA UDI In Commercial Distribution 🇺🇸 United States

Tibial augment, Screw locking

DI: 04712771480368 · Model: 2803-5211 · UNITED ORTHOPEDIC CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tibial augment, Screw locking
Primary DI
04712771480368
Version / Model
2803-5211
Catalog Number
2803-5211
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2018-07-18
Public Version Status
Update
Public Device Record Key
adb20399-f7f5-485a-941c-bb9b32a5b662

Device Description

Tibial augment, Screw locking, #1, 5mm

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

GMDN Terms

Code Name
33665 Posterior-stabilized total knee prosthesis

Identifiers

Type ID
Primary 04712771480368

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082424 000

Device Sizes

Type Value Unit Text
Device Size Text, specify #1