# K060888: Acell Powder Wound Dressing

- Pathway: 510(k) (Traditional)
- Applicant: Acell, Inc.
- Decided: Jun 23, 2006 after 84 days
- Product code: KGN (Wound Dressing With Animal-Derived Material(S))
- 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: 6 generations back to K921895 (1992). 27 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021637: Acell Ubm Lyophilized Wound Dressing, Acell, Inc. (2002) Summary page 1.
- K030921: Collagen Topical Wound Dressing, Collagen Matrix, Inc. (2003) Summary page 1.

## Most influential descendants
- K172593: XCelliStem Wound Powder (2018), 1 descendant of its own
- K080868: Aongen Collagen Matrix (2009), 1 descendant of its own
- K232204: ReyaGel (RG03 - MTP gel 3mL) (2024), 0 descendants of its own
- K173223: ologen Collagen Matrix (2018), 0 descendants of its own
- K153754: MicroMatrix (2016), 0 descendants of its own

## Indications for use
The ACell Powder Wound Dressing is intended for the management of topical wounds including: 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, second-degree burns, and skin tears), and draining wounds. The device is intended for one-time use.

Source page: https://510kreport.com/device/K060888
Methodology: https://510kreport.com/methodology