LUX Expandable Lumbar Interbody System
K-Number: K253583 · 2026-02-23
Device Summary
Frequently Asked Questions
What is the LUX Expandable Lumbar Interbody System?
LUX Expandable Lumbar Interbody System is a medical device that received FDA 510(k) clearance on 2026-02-23. The listed applicant is Xenix Medical. The 510(k) number is K253583.
When did LUX Expandable Lumbar Interbody System receive FDA 510(k) clearance?
LUX Expandable Lumbar Interbody System received FDA 510(k) clearance on 2026-02-23, under 510(k) number K253583.
Who is the listed applicant for LUX Expandable Lumbar Interbody System?
The FDA 510(k) record lists Xenix Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUX Expandable Lumbar Interbody System?
The FDA product code for LUX Expandable Lumbar Interbody System is MAX.
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.
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.