FDA 510(k)

Lucent® XP

K-Number: K234150 · 2024-03-27

Decision Date2024-03-27

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Lucent® XP is a medical device manufactured by Spinal Elements. It received FDA 510(k) clearance on 2024-03-27 under approval 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. It is manufactured by Spinal Elements. The 510(k) number is K234150.

When was Lucent® XP approved by the FDA?

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

What company makes Lucent® XP?

Lucent® XP is manufactured by Spinal Elements.

What is the FDA product code for Lucent® XP?

The FDA product code for Lucent® XP is MAX.

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Official Source

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