FDA UDI In Commercial Distribution 🇺🇸 United States

InterFuse T

DI: 00819475010564 · Model: 9091-09-20-10 · VERTEBRAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
InterFuse T
Primary DI
00819475010564
Version / Model
9091-09-20-10
Catalog Number
9091-09-20-10
Company Name
VERTEBRAL TECHNOLOGIES, INC.
Labeler DUNS
362264421
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-15
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
66ff5dbb-895c-4cfc-90c0-0b50a683b637

Device Description

Intervertebral Body Fusion Device

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
MR Safe
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
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00819475010564

Customer Contacts

Phone
952-912-5400

Device Sizes

Type Value Unit Text
Height 9 Millimeter
Length 20 Millimeter
Angle 10 degree

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Ambient temperatures in a clean dry area