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PICO 7 Single Use Negative Pressure Wound Therapy System, PICO 14 Single Use Negative Pressure Wound Therapy System, PICO Fluid Management Packs

K211318 Class II Traditional
Decision Date
2022-01-05
Sponsor / Applicant
Smith Nephew Medical Limited

Technical Specification

510(k) Submission ID K211318
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2022-01-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICO 7 Single Use Negative Pressure Wound Therapy System, PICO 14 Single Use Negative Pressure Wound Therapy System, PICO Fluid Management Packs received FDA 510(k) clearance under submission number K211318, sponsored by Smith Nephew Medical Limited. 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 2022-01-05.

Classification & Regulation

This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.