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FDA 510(k)

SIRION Lateral Lumbar Interbody System

K-Number: K223335 · 2023-05-09

ApplicantAstura Medical
Decision Date2023-05-09
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SIRION Lateral Lumbar Interbody System is the device name listed in this FDA 510(k) record. The listed applicant is Astura Medical. It received FDA 510(k) clearance on 2023-05-09 under 510(k) number K223335. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRION Lateral Lumbar Interbody System?

SIRION Lateral Lumbar Interbody System is a medical device that received FDA 510(k) clearance on 2023-05-09. The listed applicant is Astura Medical. The 510(k) number is K223335.

When did SIRION Lateral Lumbar Interbody System receive FDA 510(k) clearance?

SIRION Lateral Lumbar Interbody System received FDA 510(k) clearance on 2023-05-09, under 510(k) number K223335.

Who is the listed applicant for SIRION Lateral Lumbar Interbody System?

The FDA 510(k) record lists Astura Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIRION Lateral Lumbar Interbody System?

The FDA product code for SIRION Lateral Lumbar Interbody System is MAX.

Related Clinical Trials

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NCT06904898CONDUIT vs. PEEK CagesACTIVE_NOT_RECRUITING

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Related Devices (Code: MAX)

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.

K261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SySeaSpine Orthopedics CorporationK253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.K261159Exceed® Biplanar Expandable Interbody SystemSpine Wave, Inc.

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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