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: HWE FDA class 1

Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

General, Plastic Surgery

View full classification →

An AC-powered motor surgical instrument and accessory/attachment is an electrically powered orthopedic surgical tool used for drilling, sawing, reaming, or driving implants during surgical procedures, along with associated accessories. It is classified as an FDA Class 1 device under 21 CFR 878.4820, indicating low risk and general controls only. Product code HWE falls under the General and Plastic Surgery medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
IntelliSense Drill
ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRES
SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBE
EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEM
SYNTHES (USA) ELECTRIC PEN DRIVE SYSTEM
REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS
REPROCESSED USED, DISPOSABLE BLADES, BURS, BITS AND TAPS
REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS
AVCORE SYSTEM
AESCULAP HILAN MOTOR SYSTEM
BONE GRAFT HARVESTER
SURGICAL BURS AND SURGICAL DRILL BITS
DISK WHISK CUTTING DEVICE (CONICAL, ELLIPTICAL AND BALL HEAD)
SYNTHES (USA) COMPACT AIR DRIVE II (CAD II)
SERVOTRONIC EC100 SYSTEM
RIWO DRIVE WITH FOOTSWITCH/MOTOR HANDLE, COOMPLETE,6000RPM/3000RPM/ROTARY BLADES AND ABRADERS SEE SECTION 1:
SPINE-TECH BONE HARVESTER
MEDNEXT SURGICAL BUR
SYNTHES STERILE DRILL BITS
STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES
CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER
POWERCUT GOLD SURGICAL SYSTEM
COMMAND 2 MICOELECTRIC SURGICAL SYSTEM
CEMENT AND BONE REMOVAL KIT
EXACTECH STERILE MODULAR DRILL BIT
HALL MODULAR ACETABULAR REAMER SYSTEM
AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON)
3M MINI-DRIVER ELECTRIC SYSTEM
MICROAIRE SMARTDRIVE SYSTEM
GRAFTOLOGER PGH & ACL RECONSTRUCTION INSTRUMENT SET
CONSENSUS(TM) ORTHOPEDIC DRILL BIT
CONSENSUS(TM) PATELLA REAMER
CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER
CONSENUS HIP SYSTEM -- ACETABULAR REAMER
CONSENSUS HIP SYSTEM -- TROCHANTERIC CUTTER
CONSENSUS HIP SYSTEM -- CALCAR PLANER
STRYKER TOTAL PERFORMANCE SYSTEM
COHORT BONE BRUSH
SURGICAL INSTRUMENTS AND ACCESSORIES
HALL MICROCHOICE ELECTRIC POWERED SYSTEM
TOTAL KNEE KIT
COOL CUT
THE GRAFTOLOGER
INTERMEDICS ORTHOPEDICS DRILL BITS
SNAP BONE REAMER
SNAP DRILL
BONE SAW BLADES
ARTHREX AR-8200 SHAVER SYSTEM
SODEM POWER SYSTEM
POWERED SURGICAL INSTRUMENT ACCESSORY

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.

Popular Product Codes

Commonly searched