FDA UDI In Commercial Distribution 🇺🇸 United States

Irix-A Lumbar Integrated Fusion System

DI: M697C0803326131 · Model: C080-332613 · Xtant Medical Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Irix-A Lumbar Integrated Fusion System
Primary DI
M697C0803326131
Version / Model
C080-332613
Company Name
Xtant Medical Holdings, Inc.
Labeler DUNS
081224143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-30
Public Version
5
Public Version Date
2021-06-03
Public Version Status
Update
Public Device Record Key
58882d9f-0d82-4df2-9d45-9d91a5ff0a7c

Device Description

332613 GUIDED INSERTER, ASSEMBLY

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
HWA IMPACTOR

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Direct Marking M697C0803326130
Primary M697C0803326131

Customer Contacts