FDA UDI In Commercial Distribution 🇺🇸 United States

FortiFix

DI: 00814216026798 · Model: NV-908-1209 · NANOVIS SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FortiFix
Primary DI
00814216026798
Version / Model
NV-908-1209
Catalog Number
NV-908-1209
Company Name
NANOVIS SPINE, LLC
Labeler DUNS
079898044
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-28
Public Version
3
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
3af09e60-9d39-410c-9de8-c3b7df0c9a8f

Device Description

Nano FortiFix MIS implant tray

Device Characteristics

Single Use
No
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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00814216026798

Customer Contacts

Phone
8779076266

Premarket Submissions

Submission Number Supplement Number
K203452 000