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Model note · Cranial Drill

Stryker CORE 2 Console

Stryker's CORE platform powers its neuro, spine and ENT drills from one console. The CORE 2 console has a touchscreen, RFID recognition of accessories and an integrated irrigation pump, and drives handpieces such as the Sumex high speed drill used for craniotomy and skull base work. The console itself has no patient contact and is not field repairable.

The model

Maker, model and type.

Maker
Stryker Instruments (Stryker Corporation)
Model
CORE 2 Console (5400-052-000) with CORE Sumex high speed drill (5400-130-000)
Device type
Cranial Drill
Main document
Open the public document

Key specifications

What the public record says.

ItemValueSource
Console power100 to 240 V, 50/60 Hz, 6 to 3 A input; motor port 40 V; footswitch port 5 VSource
Console size and weight330 x 137 x 442 mm (W x H x D); 7.8 kgSource
Fuses2 x 6.3 A, 250 VAC, 5 x 20 mm, fast acting, low breaking capacitySource
Electrical class and ingressClass I, Type BF applied part; IPX0Source
Mode of operationContinuous operation with intermittent loading; duty cycles set by each motor's IFUSource
Irrigation pumpDC brush motor with optical encoder driving a peristaltic pump under microcontroller speed controlSource
Sumex drill speed75,000 RPM with electronic torque feedback that raises output under loadSource
Sumex compatible cuttersZyphr, Elite and MIS burs; SD/PD and Maestro attachmentsSource
FDA clearanceK171840, product code ERL, cleared September 2017Source

Recalls

Recalls.

This note lists no recalls. Check the FDA recall database for the latest record.

Safety

Safety warnings from the record.

  • Do not use the console in an MRI environment. Source
  • Place footswitches where they cannot be pressed by accident. Source
  • Select the correct attachment or reducer in the motor settings, or the speed shown and delivered may be wrong. Source
  • Follow each motor's duty cycle to avoid overheating. Source
  • Power remains present in standby; unplug the cord to remove power fully. Source

Sources

Where this note comes from.

Not covered: The CORE 2 IFU gives troubleshooting by symptom but no numbered error codes, so none are listed. The Sumex handpiece IFU, its duty cycle and cleaning details were not opened; Sumex data comes from a 2007 brochure. No FDA recall records were found for the CORE 2 console or Sumex drill through openFDA searches. The manufacturerUrl page was not opened.

BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.