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FDA 510(k)

KLS Martin IPS Forearm System

K-Number: K250865 · 2025-11-14

ApplicantKLS-Martin L.P.
Decision Date2025-11-14
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KLS Martin IPS Forearm System is a medical device manufactured by KLS-Martin L.P.. It received FDA 510(k) clearance on 2025-11-14 under approval number K250865. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLS Martin IPS Forearm System?

KLS Martin IPS Forearm System is a medical device that received FDA 510(k) clearance on 2025-11-14. It is manufactured by KLS-Martin L.P.. The 510(k) number is K250865.

When was KLS Martin IPS Forearm System approved by the FDA?

KLS Martin IPS Forearm System received FDA 510(k) clearance on 2025-11-14, under approval number K250865.

What company makes KLS Martin IPS Forearm System?

KLS Martin IPS Forearm System is manufactured by KLS-Martin L.P..

What is the FDA product code for KLS Martin IPS Forearm System?

The FDA product code for KLS Martin IPS Forearm System is HRS.

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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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