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Liberty SI

FDA UDI

Class II (US FDA UDI)

by Spinal Simplicity, LLC

Identity

Trade Name
Liberty SI FDA UDI
Generic Name
Sacroiliac joint intra-articular arthrodesis implant FDA UDI
Device Name
Lateral SI Joint Fusion Implant 10mm Size D FDA UDI
Model / Reference
10-0123-000 FDA UDI
Description
Lateral SI Joint Fusion Implant 10mm Size D FDA UDI

Identifiers

Primary DI / UDI-DI
M9431001230000 FDA UDI
510(k) Number
K231923 FDA UDI
FDA Product Code
OUR FDA UDI
GMDN Term
Sacroiliac joint intra-articular arthrodesis implant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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: Sacroiliac joint intra-articular arthrodesis implant

Liberty SI by Spinal Simplicity, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sacroiliac joint intra-articular arthrodesis implant.

Cleared under the same submission

K231923 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spinal Simplicity, LLC

Sources (1)

  • FDA UDI 9d92bf23-0bc4-4d70-8b47-e5d0afb71307 34 fields · synced Jun 9, 2026