SiOxD® Wound Matrix
K-Number: K241660 · 2024-07-05
Device Summary
Frequently Asked Questions
What is the SiOxD® Wound Matrix?
SiOxD® Wound Matrix is a medical device that received FDA 510(k) clearance on 2024-07-05. It is manufactured by Sioxmed, LLC. The 510(k) number is K241660.
When was SiOxD® Wound Matrix approved by the FDA?
SiOxD® Wound Matrix received FDA 510(k) clearance on 2024-07-05, under approval number K241660.
What company makes SiOxD® Wound Matrix?
SiOxD® Wound Matrix is manufactured by Sioxmed, LLC.
What is the FDA product code for SiOxD® Wound Matrix?
The FDA product code for SiOxD® Wound Matrix is QSZ.
Related Clinical Trials
Other Devices by Sioxmed, LLC
Related Devices (Code: QSZ)
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.