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Axle Interspinous Fusion System

FDA UDI

Class II (US FDA UDI)

by Xtant Medical Holdings, Inc.

Identity

Trade Name
Axle Interspinous Fusion System FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
IRIX-A INTEGRATED SPACER, TITANIUM, 38 X 28 X 12°, 17mm (STERILE) FDA UDI
Model / Reference
X080-382817-12T-STR FDA UDI
Description
IRIX-A INTEGRATED SPACER, TITANIUM, 38 X 28 X 12°, 17mm (STERILE) FDA UDI

Identifiers

Primary DI / UDI-DI
M697X08038281712TSTR1 FDA UDI
FDA Product Code
OVD FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 28 Millimeter FDA UDI
Height — 17 Millimeter FDA UDI
Angle — 12 degree FDA UDI
Width — 38 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

Axle Interspinous Fusion System by Xtant Medical Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95ace442-6d3b-4b28-b978-695d2af0e5bd 35 fields · synced Jun 8, 2026