# K112341: Snap Wound Care System

- Pathway: 510(k) (Special)
- Applicant: Spiracur, Inc.
- Decided: Aug 29, 2011 after 14 days
- Product code: OKO (Negative Pressure Wound Therapy Non-Powered Suction Apparatus)
- Device class: 2
- Regulation: 21 CFR 878.4683
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to DEN080011 (2009). 2 ancestors in all.
14 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111393: Snap (R) Wound Care System, Spiracur, Inc. (2011)

## Most influential descendants
- K132080: Snap Wound Care System (2014), 12 descendants of its own
- K142272: SNaP Wound Care System (2014), 11 descendants of its own
- K151710: SNaP Wound Care System (2015), 10 descendants of its own
- K200305: NPseal (2020), 6 descendants of its own
- K211130: NPseal (2021), 5 descendants of its own

## Indications for use
The SNaP® Wound Care System is indicated for patients who would benefit from a suction device, particularly as the device may promote wound healing through the removal of excess exudates, infectious material and tissue debris. The SNaP Wound Care System is indicated for removal of small amounts of exudate from chronic, acute, traumatic, subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), surgically closed incisions, flaps and grafts.

Source page: https://510kreport.com/device/K112341
Methodology: https://510kreport.com/methodology