FDA UDI Not in Commercial Distribution 🇺🇸 United States

PROFIX

DI: 03596010488541 · Model: 71523257 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROFIX
Primary DI
03596010488541
Version / Model
71523257
Catalog Number
71523257
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
7daa8cb6-12ea-4231-a4df-8867c00f1a49
Distribution End Date
2016-07-12

Device Description

PROFIX OXINIUM POSTERIOR STABILIZED FEM SZ 5 LT

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

GMDN Terms

Code Name
34195 Unicondylar knee prosthesis

Identifiers

Type ID
Primary 03596010488541

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K962557 000