FDA UDI In Commercial Distribution 🇺🇸 United States

TOWNLEY™ Transfacetpedicular Screw Fixation System

DI: 00613994723260 · Model: X0509523 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TOWNLEY™ Transfacetpedicular Screw Fixation System
Primary DI
00613994723260
Version / Model
X0509523
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
05d6e12d-e496-4fa3-8aa9-d90f2518e7f5

Device Description

SCREW X0509523 CORTICAL TI 3.5X26

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MRW SYSTEM, FACET SCREW SPINAL DEVICE

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00613994723260

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K021705 000

Device Sizes

Type Value Unit Text
Length 26.0 Millimeter
Outer Diameter 3.5 Millimeter