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FDA 510(k)

Lucent® XP

K-Number: K234150 · 2024-03-27

ApplicantSpinal Elements
Decision Date2024-03-27
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Lucent® XP is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Elements. It received FDA 510(k) clearance on 2024-03-27 under 510(k) number K234150. 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 Lucent® XP?

Lucent® XP is a medical device that received FDA 510(k) clearance on 2024-03-27. The listed applicant is Spinal Elements. The 510(k) number is K234150.

When did Lucent® XP receive FDA 510(k) clearance?

Lucent® XP received FDA 510(k) clearance on 2024-03-27, under 510(k) number K234150.

Who is the listed applicant for Lucent® XP?

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

What is the FDA product code for Lucent® XP?

The FDA product code for Lucent® XP is MAX.

Other records listing Spinal Elements as applicant

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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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