FDA UDI In Commercial Distribution 🇺🇸 United States

VertebraLINK

DI: 00817329021827 · Model: 84-0007/1006 · LINKSPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VertebraLINK
Primary DI
00817329021827
Version / Model
84-0007/1006
Catalog Number
84-0007/1006
Company Name
LINKSPINE, INC.
Labeler DUNS
067584601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-18
Public Version
5
Public Version Date
2018-11-27
Public Version Status
Update
Public Device Record Key
d58df987-d237-4489-b826-72a0f5d2ddfa

Device Description

10 x 30 x 10 x 6 PLIF IBD

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 00817329021827

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162693 000

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Width 10 Millimeter
Angle 6 degree
Height 10 Millimeter