FDA UDI In Commercial Distribution 🇺🇸 United States

Axle Interspinous Fusion System

DI: M697X06012171 · Model: X060-1217 · Xtant Medical Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Axle Interspinous Fusion System
Primary DI
M697X06012171
Version / Model
X060-1217
Company Name
Xtant Medical Holdings, Inc.
Labeler DUNS
081224143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-17
Public Version
4
Public Version Date
2021-06-03
Public Version Status
Update
Public Device Record Key
28add1c9-3a60-48ac-93c0-308ee695179c

Device Description

AXLE-X LOCKING PLATE ASSEMBLY, 37MM, 10MM

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
Yes
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
PEK Spinous process plate

GMDN Terms

Code Name
61532 Lumbar interspinous decompression spacer, non-sterile

Identifiers

Type ID
Primary M697X06012171

Customer Contacts

Device Sizes

Type Value Unit Text
Width 10 Millimeter
Length 37 Millimeter