FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERTEX® Reconstruction System

DI: 00613994204103 · Model: 7750090 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VERTEX® Reconstruction System
Primary DI
00613994204103
Version / Model
7750090
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-08
Public Version
4
Public Version Date
2018-11-09
Public Version Status
Update
Public Device Record Key
256661e0-a475-433f-a82a-3abd02aa1895
Distribution End Date
2018-10-24

Device Description

ROD 7750090 3.75MM ROD 120MM

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary 00613994204103

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070742 000

Device Sizes

Type Value Unit Text
Length 120.0 Millimeter