FDA UDI In Commercial Distribution 🇺🇸 United States

AxTiHA®

DI: M711AXTI1836200 · Model: AXTi183620 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AxTiHA®
Primary DI
M711AXTI1836200
Version / Model
AXTi183620
Catalog Number
AXTi183620
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-31
Public Version
4
Public Version Date
2023-10-30
Public Version Status
Update
Public Device Record Key
90809a47-5b69-4dd0-816c-895680e1aaf2

Device Description

Ti 6Al 4V (ELI); Hydroxyapatite

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Package M711AXTI1836201
Primary M711AXTI1836200

Customer Contacts

Phone
801-261-2236

Device Sizes

Type Value Unit Text
Height 18 Millimeter
Width 36 Millimeter
Angle 20 degree