Cleared Traditional

K170284 - Great Basin Bordetella Direct Test

K170284 is the FDA 510(k) clearance for Great Basin Bordetella Direct Test by Great Basin Scientific, Inc.. It is a Class 2 Microbiology device (product code OZZ) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K170284 · Great Basin Scientific, Inc. · Microbiology device
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Mar 2017
Decision
60d
Days
Class 2
Risk

K170284 is an FDA 510(k) clearance for the Great Basin Bordetella Direct Test. Classified as Bordetella Pertussis Dna Assay System (product code OZZ), Class II - Special Controls.

Submitted by Great Basin Scientific, Inc. (Salt Lake City, US). The FDA issued a Cleared decision on March 31, 2017 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3980 - the FDA microbiology 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Great Basin Scientific, Inc. devices

Submission Details

510(k) Number K170284 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 2017
Decision Date March 31, 2017
Days to Decision 60 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 102d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code OZZ Bordetella Pertussis Dna Assay System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.3980
Definition A Qualitative In Vitro Diagnostic Assay Intended To Detect Bordetella Pertussis Dna Extracted From Human Respiratory Specimens. Detection Of Bordetella Pertussis Dna Aids In The Diagnosis Of Bordetella Pertussis Respiratory Infection In Conjunction With Other Clinical And Laboratory Testing In Patients Exhibiting Signs And Symptoms Of Upper Respiratory Tract Infection.
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 Microbiology devices follow this clearance model.

Regulatory Peers - OZZ Bordetella Pertussis Dna Assay System

All 7
Devices cleared under the same product code (OZZ) and FDA review panel - the closest regulatory comparables to K170284.
Simplexa Bordetella Direct, Simplexa Bordetella Positive Control Pack
K183223 · Diasorin Molecular, LLC · Dec 2018
Simplexa Bordetella Direct, Simplexa Bordetella Positive Control Pack
K173498 · Diasorin Molecular, LLC · Aug 2018
Solana Bordetella Complete Assay
K181029 · Quidel Corporation · Jul 2018
illumigene Pertussis DNA Amplification Assay
K152285 · Meridian Bioscience, Inc. · Nov 2015
AmpliVue Bordetella Assay
K143206 · Quidel Corporation · Dec 2014
ILLUMIGENE PERTUSIS DNA AMPLIFICATION ASSAY, ILLUMIGENE PERTUSSIS EXTERNAL CONTROL KIT, ILLUMIPRO-10 AUTOMATED ISOTHERMA
K133673 · Meridian Bioscience, Inc. · Mar 2014