Cleared Traditional

K200723 - StealthStation FlexENT (9736242), StealthStation S8 ENT Software (9735762) (FDA 510(k) Clearance)

Jun 2020
Decision
99d
Days
Class 2
Risk

K200723 is an FDA 510(k) clearance for the StealthStation FlexENT (9736242), StealthStation S8 ENT Software (9735762). This device is classified as a Ear, Nose, And Throat Stereotaxic Instrument (Class II - Special Controls, product code PGW).

Submitted by Medtronic Navigation, Inc. (Louisville, US). The FDA issued a Cleared decision on June 26, 2020, 99 days after receiving the submission on March 19, 2020.

This device falls under the Ear, Nose, Throat FDA review panel. Regulated under 21 CFR 882.4560. Intended As An Aid For Precisely Locating A Surgical Instrument Within Anatomical Structures In Either Open Or Percutaneous Procedures For Any Medical Condition In Which A Reference To A Rigid Anatomical Structure In The Field Of Ent Surgery Can Be Identified Relative To A Ct- Or Mr-based Model Or Digitized Landmarks Of The Anatomy..

Submission Details

510(k) Number K200723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 2020
Decision Date June 26, 2020
Days to Decision 99 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF

Device Classification

Product Code PGW — Ear, Nose, And Throat Stereotaxic Instrument
Device Class Class II - Special Controls
CFR Regulation 21 CFR 882.4560
Definition Intended As An Aid For Precisely Locating A Surgical Instrument Within Anatomical Structures In Either Open Or Percutaneous Procedures For Any Medical Condition In Which A Reference To A Rigid Anatomical Structure In The Field Of Ent Surgery Can Be Identified Relative To A Ct- Or Mr-based Model Or Digitized Landmarks Of The Anatomy.