meddevicedb.com FDA Device Reference

SNaP Wound Care System

K142272 Class II Traditional
Decision Date
2014-11-25
Sponsor / Applicant
Spiracur, Inc.

Technical Specification

510(k) Submission ID K142272
Product Code OKO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4683
Decision Date 2014-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SNaP Wound Care System received FDA 510(k) clearance under submission number K142272, sponsored by Spiracur, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2014-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code OKO and 21 CFR 878.4683, within the General, Plastic Surgery review panel as a Class II device.