FDA UDI In Commercial Distribution 🇺🇸 United States

Triathlon

DI: 07613327015409 · Model: 5542-A-501 · Howmedica Osteonics Corp.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Triathlon
Primary DI
07613327015409
Version / Model
5542-A-501
Catalog Number
5542-A-501
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
4
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
9750b760-d97a-4baa-9437-71dd56744f5c

Device Description

Femoral Distal Augment

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
48067 Knee arthroplasty wedge

Identifiers

Type ID
Primary 07613327015409

Device Sizes

Type Value Unit Text
Device Size Text, specify Side: LEFT
Device Size Text, specify Size: 5
Device Size Text, specify Thickness: 15.0 Millimeter