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FDA 510(k)

Liberty SI Lateral Implant System

K-Number: K231923 · 2023-12-05

ApplicantSpinal Simplicity, LLC
Decision Date2023-12-05
Product CodeOUR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Liberty SI Lateral Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Simplicity, LLC. It received FDA 510(k) clearance on 2023-12-05 under 510(k) number K231923. The device is classified under product code OUR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Liberty SI Lateral Implant System?

Liberty SI Lateral Implant System is a medical device that received FDA 510(k) clearance on 2023-12-05. The listed applicant is Spinal Simplicity, LLC. The 510(k) number is K231923.

When did Liberty SI Lateral Implant System receive FDA 510(k) clearance?

Liberty SI Lateral Implant System received FDA 510(k) clearance on 2023-12-05, under 510(k) number K231923.

Who is the listed applicant for Liberty SI Lateral Implant System?

The FDA 510(k) record lists Spinal Simplicity, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Liberty SI Lateral Implant System?

The FDA product code for Liberty SI Lateral Implant System is OUR.

Other records listing Spinal Simplicity, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253523Freedom DS™ Decompression SystemK253250Minuteman® G6 MIS Fusion PlateK250001Patriot SI Implant SystemK240592Wolff's Law Anterior Cervical Plate SystemK232259Patriot-SI Posterior Implant SystemK234051Minuteman G5 MIS Fusion Plate; Minuteman G1(Posterior Fusion Plate /HA Posterior Fusion Plate); HA Minuteman G3-R MIS Fusion Plate; Minuteman G3/HA Minuteman G3

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Related Devices (Code: OUR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260477CATAMARAN™ SI Joint Fusion SystemTenon MedicalK253488iFuse INTRA Ti™ Implant SystemSI-BONE, Inc.K253611Falco Fusion SystemMcnicoll Surgical, Inc.K252834Sacroiliac Joint Truss System (SJTS)4Web MedicalK251365OptumSI Implant SystemSi Solutions, LLCK252322SIros-X SystemGenesys Spine

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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