# K142272: SNaP Wound Care System

- Pathway: 510(k) (Traditional)
- Applicant: Spiracur, Inc.
- Decided: Nov 25, 2014 after 102 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: 4 generations back to DEN080011 (2009). 4 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132080: Snap Wound Care System, Spiracur, Inc. (2014) Summary page 5.

## Most influential descendants
- 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
- K212971: NPseal (2022), 4 descendants of its own
- K240244: NPseal (Small, Medium, Large) (2024), 3 descendants of its own

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

Source page: https://510kreport.com/device/K142272
Methodology: https://510kreport.com/methodology