FDA UDI In Commercial Distribution 🇺🇸 United States

FortiCore®

DI: 00814216022509 · Model: 11302-2911N · NANOVIS SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FortiCore®
Primary DI
00814216022509
Version / Model
11302-2911N
Catalog Number
11302-2911N
Company Name
NANOVIS SPINE, LLC
Labeler DUNS
079898044
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-22
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
960d1bef-4265-4460-b991-0948c28b0c4f

Device Description

FortiCore® TLIF Spacer 11x13x29, 6 degree

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
61230 Metal-polymer composite spinal interbody fusion cage

Identifiers

Type ID
Primary 00814216022509

Customer Contacts

Phone
877-907-6266

Device Sizes

Type Value Unit Text
Width 13 Millimeter
Length 29 Millimeter
Height 11 Millimeter