FDA UDI In Commercial Distribution 🇺🇸 United States

ATTUNE

DI: 10603295520702 · Model: 1514-01-500 · DEPUY (IRELAND)
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATTUNE
Primary DI
10603295520702
Version / Model
1514-01-500
Catalog Number
151401500
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-30
Public Version
1
Public Version Date
2023-07-10
Public Version Status
New
Public Device Record Key
42f5abf1-da86-4bd6-8de8-02f4885633e4

Device Description

ATTUNE KNEE SYSTEM REVISION FEMORAL CONE XX-LARGE

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
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

GMDN Terms

Code Name
61556 Sleeve femoral/tibial extension, coated

Identifiers

Type ID
Primary 10603295520702

Customer Contacts