K-number	K252610
Device name	ZSFab Lumbar Interbody System
Applicant	Zsfab, Inc.
Product code	MAX
Device class	Class II
Decision date	Nov 25, 2025
Decision	Substantially Equivalent
Regulation	888.3080

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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ZSFab Lumbar Interbody System

Everything you need for a 510(k) submission. Nothing you don't.