Cleared Traditional

K963246 - TREBAY MICRODEBRIDER OR XPS STRAIGHT SHOT (FDA 510(k) Clearance)

Sep 1996
Decision
35d
Days
Class 2
Risk

K963246 is an FDA 510(k) clearance for the TREBAY MICRODEBRIDER OR XPS STRAIGHT SHOT. This device is classified as a Drill, Surgical, Ent (electric Or Pneumatic) Including Handpiece (Class II - Special Controls, product code ERL).

Submitted by Medtronic Xomed (Jacksonville, US). The FDA issued a Cleared decision on September 23, 1996, 35 days after receiving the submission on August 19, 1996.

This device falls under the Ear, Nose, Throat FDA review panel. Regulated under 21 CFR 874.4250.

Submission Details

510(k) Number K963246 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 19, 1996
Decision Date September 23, 1996
Days to Decision 35 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF

Device Classification

Product Code ERL - Drill, Surgical, Ent (electric Or Pneumatic) Including Handpiece
Device Class Class II - Special Controls
CFR Regulation 21 CFR 874.4250