FDA UDI In Commercial Distribution 🇺🇸 United States

CD Horizon™ ModuLeX™ Spinal System

DI: 20763000591827 · Model: 55946205555 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
CD Horizon™ ModuLeX™ Spinal System
Primary DI
20763000591827
Version / Model
55946205555
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2022-12-11
Public Version
1
Public Version Date
2022-12-19
Public Version Status
New
Public Device Record Key
b363338a-0f61-4457-9754-9a07d9f47c7d

Device Description

SCREW PK 55946205555 S MX FAS 5.5X55 2PK

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWQ Appliance, fixation, spinal intervertebral body
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Unit of Use 00763000591823
Primary 20763000591827

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K221244 000