Cleared Traditional

K860460 - MICROTEK STAINLESS STEEL PISTON

K860460 is the FDA 510(k) clearance for MICROTEK STAINLESS STEEL PISTON by Microtek Medical, Inc.. It is a Class 2 Ear, Nose, Throat device (product code ETB) cleared through the Traditional 510(k) pathway after a 155-day FDA review.

K860460 · Microtek Medical, Inc. · Ear, Nose, Throat device
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Jul 1986
Decision
155d
Days
Class 2
Risk

K860460 is an FDA 510(k) clearance for the MICROTEK STAINLESS STEEL PISTON. Classified as Prosthesis, Partial Ossicular Replacement (product code ETB), Class II - Special Controls.

Submitted by Microtek Medical, Inc. (Columbus, US). The FDA issued a Cleared decision on July 11, 1986 after a review of 155 days - an extended review cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.3450 - the FDA ear, nose and throat device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ear, Nose, Throat review framework, consistent with the majority of Class II 510(k) submissions.

View all Microtek Medical, Inc. devices

Submission Details

510(k) Number K860460 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 06, 1986
Decision Date July 11, 1986
Days to Decision 155 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d slower than avg
Panel avg: 89d · This submission: 155d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code ETB Prosthesis, Partial Ossicular Replacement
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.3450
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Ear, Nose, Throat devices follow this clearance model.

Regulatory Peers - ETB Prosthesis, Partial Ossicular Replacement

All 30
Devices cleared under the same product code (ETB) and FDA review panel - the closest regulatory comparables to K860460.
XOMED PLATINUM WIRE TEFLON PISTION
K872112 · Xomed, Inc. · Jul 1987
PROSTHESIS WIRE
K870766 · Treace Medical, Inc. · Apr 1987
INCUS/STAPES PROSTHESIS
K861369 · Richards Medical Co., Inc. · Jul 1986
INCUS PROSTHESIS
K844961 · Richards Medical Co., Inc. · Feb 1985
CAUSSE SPONGE BOAT
K841353 · Treace Medical, Inc. · Jul 1984
FISCH MODIFIED TEF-WIRE PISTON
K823429 · Treace Medical, Inc. · Dec 1982