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FDA 510(k)

Marrow Marxman

K-Number: K260572 · 2026-08-04

ApplicantMedimetrix, LLC
Decision Date2026-08-04
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Marrow Marxman is the device name listed in this FDA 510(k) record. The listed applicant is Medimetrix, LLC. It received FDA 510(k) clearance on 2026-08-04 under 510(k) number K260572. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Marrow Marxman?

Marrow Marxman is a medical device that received FDA 510(k) clearance on 2026-08-04. The listed applicant is Medimetrix, LLC. The 510(k) number is K260572.

When did Marrow Marxman receive FDA 510(k) clearance?

Marrow Marxman received FDA 510(k) clearance on 2026-08-04, under 510(k) number K260572.

Who is the listed applicant for Marrow Marxman?

The FDA 510(k) record lists Medimetrix, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Marrow Marxman?

The FDA product code for Marrow Marxman is KNW.

Related Devices (Code: KNW)

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.

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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.

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