FDA UDI In Commercial Distribution 🇺🇸 United States

Vertex Reconstruction System

DI: 00613994641670 · Model: G7750020 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vertex Reconstruction System
Primary DI
00613994641670
Version / Model
G7750020
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-18
Public Version
1
Public Version Date
2021-09-27
Public Version Status
New
Public Device Record Key
9d9039c1-cccd-4c95-a39a-5525b0dca614

Device Description

ROD G7750020 TI 3.5 X 300MM

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
Yes
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
Radiation Sterilization

Product Codes

Code Name
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKG Posterior cervical screw system

GMDN Terms

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

Identifiers

Type ID
Primary 00613994641670

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180851 000