Cleared Traditional

Smith & Nephew Tablet Application

K190367 · Smith & Nephew · General & Plastic Surgery
May 2019
Decision
95d
Days
Class 2
Risk

About This 510(k) Submission

K190367 is an FDA 510(k) clearance for the Smith & Nephew Tablet Application, a Mobile / Tablet Software Application To Control Settings Of Surgical And Endoscopic Camera (Class II — Special Controls, product code QGY), submitted by Smith & Nephew (Andover, US). The FDA issued a Cleared decision on May 21, 2019, 95 days after receiving the submission on February 15, 2019. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K190367 FDA.gov
FDA Decision Cleared SESE
Date Received February 15, 2019
Decision Date May 21, 2019
Days to Decision 95 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code QGY — Mobile / Tablet Software Application To Control Settings Of Surgical And Endoscopic Camera
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition Device Is Intended For Wireless Control Of Settings For Surgical Or Endoscopic Camera Control Unit And Patient Information System.