FDA 510(k)

Marrow Marxman

Numéro K : K260572 · 2026-08-04

Date de décision2026-08-04

Code produitKNW

Comité consultatifGU

DécisionSubstantially Equivalent

Résumé du dispositif

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.

Questions fréquentes

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.

Essais cliniques associés

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Dispositifs connexes (Code : KNW)

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Source officielle

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