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Australis ALIF Cage

FDA UDI

Class II (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Australis ALIF Cage FDA UDI
Generic Name
Metal-polymer composite spinal interbody fusion cage FDA UDI
Model / Reference
131-07-1203 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215127930 FDA UDI
510(k) Number
K172019 FDA UDI
FDA Product Code
OVD FDA UDI
GMDN Term
Metal-polymer composite 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Metal-polymer composite spinal interbody fusion cage

Australis ALIF Cage by Signature Orthopaedics Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metal-polymer composite spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b52d8db-ae56-49ad-810a-b2259f5593fc 33 fields · synced Jun 6, 2026