FDA UDI In Commercial Distribution 🇺🇸 United States

OTHER EXTERNAL FIXATION

DI: 03596010171252 · Model: 71031029 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OTHER EXTERNAL FIXATION
Primary DI
03596010171252
Version / Model
71031029
Catalog Number
71031029
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-25
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
8afec123-c049-4ffb-8d40-1e963f2dde02

Device Description

HYBRID STRUT

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
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

GMDN Terms

Code Name
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Primary 03596010171252

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K953397 000