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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 a medical device manufactured by Acell, Inc.. It received FDA 510(k) clearance on 2024-07-11 under approval 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. It is manufactured by Acell, Inc.. The 510(k) number is K241706.

When was MicroMatrix® UBM Particulate approved by the FDA?

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

What company makes MicroMatrix® UBM Particulate?

MicroMatrix® UBM Particulate is manufactured by Acell, Inc..

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

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

Other Devices by Acell, Inc.

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Related Devices (Code: KGN)

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.