FDA UDI In Commercial Distribution 🇺🇸 United States

JOURNEY II XR

DI: 00885556688397 · Model: 74013893 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JOURNEY II XR
Primary DI
00885556688397
Version / Model
74013893
Catalog Number
74013893
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-29
Public Version
8
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
dc9ca15f-9945-4f3a-92dc-93d8c09a50bb

Device Description

JOURNEY XR TIBIAL INSERT TRIAL SIZE 1-2 LEFT MEDIAL -2 DEGREE 12MM

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00885556688397

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K141471 000