Cleared Traditional

K003612 - MICROSPEED EC MOTORSYSTEM GD650/GD653

K003612 is an FDA 510(k) clearance for MICROSPEED EC MOTORSYSTEM GD650/GD653, manufactured by Aesculap, Inc.. The device is a Class 2 Neurology device with product code HBC cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K003612 · Aesculap, Inc. · Neurology device
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Feb 2001
Decision
90d
Days
Class 2
Risk

K003612 is an FDA 510(k) clearance for the MICROSPEED EC MOTORSYSTEM GD650/GD653. Classified as Motor, Drill, Electric (product code HBC), Class II - Special Controls.

Submitted by Aesculap, Inc. (Center Valley, US). The FDA issued a Cleared decision on February 20, 2001 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4360 - 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 Aesculap, Inc. devices

FDA 510(k) Submission Details - K003612

510(k) Number K003612 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 22, 2000
Decision Date February 20, 2001
Days to Decision 90 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 148d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HBC Device Classification - Class 2, Special Controls

Product Code HBC Motor, Drill, Electric
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4360
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 - HBC Motor, Drill, Electric

All 21
Devices cleared under the same product code (HBC) and FDA review panel - the closest regulatory comparables to K003612.
MICROSPEED UNI MOTOR SYSTEM
K053526 · Aesculap, Inc. · Jan 2006
THE BIOPLATE BATTERY POWERED DRILL
K022986 · Bioplate, Inc. · Nov 2002
ANSPACH EMAX DRILL SYSTEM
K011444 · The Anspach Effort, Inc. · Aug 2001
ADVANTAGE DRIVE SYSTEM
K002523 · Linvatec Corp. · Oct 2000
SERVOTRONIC EC100 SYSTEM
K972857 · Medicon EG · Jan 1998