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FDA 510(k)

MicroMatrix® UBM Particulate

K-Number: K241706 · 2024-07-11

ApplicantAcell, Inc.
Decision Date2024-07-11
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

MicroMatrix® UBM Particulate is the device name listed in this FDA 510(k) record. The listed applicant is Acell, Inc.. It received FDA 510(k) clearance on 2024-07-11 under 510(k) number K241706. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MicroMatrix® UBM Particulate?

MicroMatrix® UBM Particulate is a medical device that received FDA 510(k) clearance on 2024-07-11. The listed applicant is Acell, Inc.. The 510(k) number is K241706.

When did MicroMatrix® UBM Particulate receive FDA 510(k) clearance?

MicroMatrix® UBM Particulate received FDA 510(k) clearance on 2024-07-11, under 510(k) number K241706.

Who is the listed applicant for MicroMatrix® UBM Particulate?

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

What is the FDA product code for MicroMatrix® UBM Particulate?

The FDA product code for MicroMatrix® UBM Particulate is KGN.

Other records listing Acell, Inc. as applicant

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.

View all 11 devices →

Related Devices (Code: KGN)

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.

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.