FDA UDI In Commercial Distribution 🇺🇸 United States

GENESIS II

DI: 03596010000798 · Model: 71420649 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
GENESIS II
Primary DI
03596010000798
Version / Model
71420649
Catalog Number
71420649
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
6
Public Version Date
2025-12-12
Public Version Status
Update
Public Device Record Key
f7aaf960-fe51-4985-ae0c-9195adb3d4c0

Device Description

GENESIS II LONG STEM 12MM X 150MM WITH SLOT

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

GMDN Terms

Code Name
48066 Knee femur stem prosthesis

Identifiers

Type ID
Primary 03596010000798

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K953274 000