FDA UDI In Commercial Distribution 🇺🇸 United States

CorticaLINK MI

DI: 00817329022848 · Model: 80-4205/050 · LINKSPINE, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CorticaLINK MI
Primary DI
00817329022848
Version / Model
80-4205/050
Catalog Number
80-4205/050
Company Name
LINKSPINE, INC.
Labeler DUNS
067584601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-22
Public Version
3
Public Version Date
2018-11-28
Public Version Status
Update
Public Device Record Key
8697c441-af07-4424-9f65-625c0b093780

Device Description

5.0mm Titanium Rod: 50mm Curved

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
Yes
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

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

Identifiers

Type ID
Primary 00817329022848

Customer Contacts

Device Sizes

Type Value Unit Text
Length 50 Millimeter
Outer Diameter 5.0 Millimeter