# K241660: SiOxD® Wound Matrix

- Pathway: 510(k) (Special)
- Applicant: Sioxmed, LLC
- Decided: Jul 5, 2024 after 25 days
- Product code: QSZ (Absorbable Synthetic Wound Dressing)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K953781 (1995). 126 ancestors in all.
No later device cites it as a predicate yet.
0 of 127 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222189: SiOxD Wound Matrix, Sioxmed, LLC (2022) Summary page 5.
- K232847: SiOxD Wound Matrix, Sioxmed, LLC (2023) Summary page 5.

## Indications for use
The SiOxD® Wound Matrix is intended for use in the management of wounds. Wound types include: Partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/grafts, post-Moh's surgery, post laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, first degree and partial thickness burns, skin tears) and draining wounds.

Source page: https://510kreport.com/device/K241660
Methodology: https://510kreport.com/methodology