FDA UDI In Commercial Distribution 🇺🇸 United States

ATTUNE

DI: 10603295043614 · Model: 1513-14-110 · DEPUY (IRELAND)
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATTUNE
Primary DI
10603295043614
Version / Model
1513-14-110
Catalog Number
151314110
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-05
Public Version
6
Public Version Date
2021-10-11
Public Version Status
Update
Public Device Record Key
77d69c46-2318-4add-b5c0-9f7868ca6ff3

Device Description

ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 14X110MM

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
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
NJL Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing

GMDN Terms

Code Name
48066 Knee femur stem prosthesis

Identifiers

Type ID
Primary 10603295043614

Customer Contacts