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. 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.
Related Devices (Code: KGN)
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.