Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: HBC FDA class 2

Motor, Drill, Electric

Neurology

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The Electric Drill Motor is an electrically powered drive unit used to operate neurosurgical drill bits, burrs, and trephines during cranial bone procedures, providing controlled rotational speed for bone penetration with reduced risk of soft tissue injury. It is classified as a Class 2 device (moderate risk), requiring 510(k) premarket notification. The product code is HBC under regulation 21 CFR 882.4360 in the Neurology specialty. It is eligible for third-party 510(k) review.

510(k) Clearances

26 matches
K Number
Device Name
Traus SSG10 Surgical System
Traus SSG30 Surgical System
ORiGO System
Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)
hekaDrill
MR8 Drill System, Midas Rex MR8 ClearView Tools
OSSEODUO Shaver and Drill System
IPC systems, Legend EHS handpieces and Legend Stylus Touch handpiece, Microsaw handpieces,Triton electric high torque handpiece, Attachments and surgical dissecting tools
MR8 Drill System
ELAN 4 Motor System
ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS
PRIMADO2 TOTAL SURGICAL SYSTEM
D4000 DRIVE SYSTEM; D4000A DRIVE SYSTEM WITH IRRIGATION
PRIMADO
CONMED LINVATEC OSPREY DRILL SYSTEM
MICROPOWER HAND PIECE HIGH SPEED DRILL
MICROSPEED UNI MOTOR SYSTEM
THE BIOPLATE BATTERY POWERED DRILL
SODEM HIGH SPEED SYSTEM (ELECTRIC) (NEURO/SPINE SURGERY)
SODEM HIGH SPEED SYSTEM (ELECTRIC) (GENERAL ORTHOPEDICS & PLASTIC SURGERY)
ANSPACH EMAX DRILL SYSTEM
MICROSPEED EC MOTORSYSTEM GD650/GD653
ADVANTAGE DRIVE SYSTEM
SERVOTRONIC EC100 SYSTEM
SURGICAL DRILL (ELECTRIC) INCLUDING HANDPIECE
450/800 DRILL

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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