Cleared Traditional

K061224 - LAPDOC I

K061224 is an FDA 510(k) clearance for LAPDOC I, manufactured by Robodent GmbH. The device is a Class 2 Neurology device with product code HAW cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K061224 · Robodent GmbH · Neurology device
Download Printable Device Report (PDF)
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Sep 2006
Decision
127d
Days
Class 2
Risk

K061224 is an FDA 510(k) clearance for the LAPDOC I. Classified as Neurological Stereotaxic Instrument (product code HAW), Class II - Special Controls.

Submitted by Robodent GmbH (Berlin, DE). The FDA issued a Cleared decision on September 5, 2006 after a review of 127 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4560 - the FDA neurology 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 Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Robodent GmbH devices

FDA 510(k) Submission Details - K061224

510(k) Number K061224 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 01, 2006
Decision Date September 05, 2006
Days to Decision 127 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
21d faster than avg
Panel avg: 148d · This submission: 127d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 299
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