FDA UDI In Commercial Distribution 🇺🇸 United States

TxTiHA®

DI: M711TXT120933100 · Model: TXT12093310 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TxTiHA®
Primary DI
M711TXT120933100
Version / Model
TXT12093310
Catalog Number
TXT12093310
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-30
Public Version
1
Public Version Date
2021-10-08
Public Version Status
New
Public Device Record Key
bef389e3-62e5-4b48-92e1-d1deeb7dad29

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Package M711TXT120933101
Primary M711TXT120933100

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K201614 000

Device Sizes

Type Value Unit Text
Width 12 Millimeter
Height 9 Millimeter
Length 33 Millimeter
Angle 10 degree