FDA UDI In Commercial Distribution 🇺🇸 United States

Kinemax

DI: 07613327046830 · Model: 6479-5-112 · Howmedica Osteonics Corp.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kinemax
Primary DI
07613327046830
Version / Model
6479-5-112
Catalog Number
6479-5-112
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
11591221-d784-4949-b870-cfd5e4a778a3

Device Description

Low Stress Insert

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
No
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
46585 Tibial insert

Identifiers

Type ID
Primary 07613327046830

Premarket Submissions

Submission Number Supplement Number
K921640 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: SM
Device Size Text, specify Thickness: 12.0 Millimeter