K-number	K250865
Device name	KLS Martin IPS Forearm System
Applicant	KLS-Martin L.P.
Product code	HRS
Device class	Class II
Decision date	Nov 14, 2025
Decision	Substantially Equivalent
Regulation	888.3030

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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KLS Martin IPS Forearm System

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