Cleared Special

K092562 - MICROTARGETING STAR DRIVE SYSTEM, COMPONENTS

K092562 is an FDA 510(k) clearance for MICROTARGETING STAR DRIVE SYSTEM, manufactured by FHC, Inc.. The device is a Class 2 Neurology device with product code HAW cleared through the Special 510(k) pathway after a 29-day FDA review.

K092562 · FHC, Inc. · Neurology device
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Sep 2009
Decision
29d
Days
Class 2
Risk

K092562 is an FDA 510(k) clearance for the MICROTARGETING STAR DRIVE SYSTEM, COMPONENTS. Classified as Neurological Stereotaxic Instrument (product code HAW), Class II - Special Controls.

Submitted by FHC, Inc. (Bowdoin, US). The FDA issued a Cleared decision on September 18, 2009 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4560 - the FDA neurology device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all FHC, Inc. devices

FDA 510(k) Submission Details - K092562

510(k) Number K092562 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 2009
Decision Date September 18, 2009
Days to Decision 29 days
Submission Type Special
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
120d faster than avg
Panel avg: 149d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

HAW Device Classification - Class 2, Special Controls

Product Code HAW Neurological Stereotaxic Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4560
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 Neurology devices follow this clearance model.

Regulatory Peers - HAW Neurological Stereotaxic Instrument

All 384
Devices cleared under the same product code (HAW) and FDA review panel - the closest regulatory comparables to K092562.
ROSA SURGICAL DEVICE, MODEL ROSA 1.1
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K080355 · Elekta Instrument AB · May 2009