MicroMatrix® UBM Particulate
K-Number: K241706 · 2024-07-11
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.