FDA UDI In Commercial Distribution 🇺🇸 United States

FORTIFY

DI: 00889095044485 · Model: 151.520 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FORTIFY
Primary DI
00889095044485
Version / Model
151.520
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-13
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
372806dc-8e19-467f-84a3-0ca7097098ee

Device Description

FORTIFY 16mm Upper Endplate, 16x20mm Footprint, 0deg, No Spikes

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00889095044485

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K112756 000

Device Sizes

Type Value Unit Text
Depth 16 Millimeter
Width 20 Millimeter