FDA UDI In Commercial Distribution 🇺🇸 United States

VertebraLINK MI

DI: 00817329023203 · Model: 84-0650 · LINKSPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VertebraLINK MI
Primary DI
00817329023203
Version / Model
84-0650
Catalog Number
84-0650
Company Name
LINKSPINE, INC.
Labeler DUNS
067584601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-29
Public Version
5
Public Version Date
2018-11-22
Public Version Status
Update
Public Device Record Key
afd60353-51f8-4c88-9467-70332fe24e55

Device Description

MI Inserter Draw Rod

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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 00817329023203

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162693 000