Cleared Traditional

K133665 - MALLEABLE SUCTION INSTRUMENTS (FDA 510(k) Clearance)

Mar 2014
Decision
104d
Days
Class 2
Risk

K133665 is an FDA 510(k) clearance for the MALLEABLE SUCTION INSTRUMENTS. 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 March 13, 2014, 104 days after receiving the submission on November 29, 2013.

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 K133665 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 29, 2013
Decision Date March 13, 2014
Days to Decision 104 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.