510(k) Report

510(k) · Cleared

Cleared

Styker Consolidated Operating Room Equipment (Core) System

K112593510(k) TraditionalCleared May 1, 2012237-day reviewClass II21 CFR 874.4250

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Stryker Corporation · ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

Cleared on May 1, 2012 after a 237-day review. The FDA summary names its predicate without a number. 20 later devices descend from it.

Decided
May 1, 2012
Review
237 days
Class
Class II
Product code
ERL
Recalls
None
Predicates
0

20 later devices descend from it, 6 citing it directly.

Descendants, by year cleared 2015: 4 descendants cleared2014: 1 descendant cleared2024: 3 descendants cleared2017: 1 descendant cleared2019: 2 descendants cleared2016: 1 descendant cleared2021: 2 descendants cleared2025: 2 descendants cleared2026: 4 descendants cleared2010201520202025
  1. This deviceK112593 Styker Consolidated Operating Room Equipment (Core) SystemStryker Corporation · 2012
  2. Descendant · cites it directly · 8 of its ownK171840 Stryker Consolidated Operating Room Equipment (CORE) 2 ConsoleStryker Corporation · 2017
  3. Descendant · 2 generations on · 7 of its ownK240662 Spine Guidance Software (version 5.0); Xia 3/ Serrato Q Instruments…Stryker Leibinger GmbH & Co KG · 2024
  4. Descendant · cites it directly · 7 of its ownK141935 Stryker S2 DrillStryker Corporation · 2014
  5. Descendant · 2 generations on · 6 of its ownK152641 Pi Drive Plus Motor, ExtenderStryker Corporation · 2015
  6. Descendant · cites it directly · 6 of its ownK143320 Stryker Elite Attachments, Stryker Heavy Duty (HD) AttachmentsStryker Corp. · 2015 · Recalled

Showing 5 of 20 descendants. See all descendants

Descendants cleared per year

2014: 12015: 42016: 12017: 12019: 22021: 22024: 32025: 22026: 4
2014high 4 (2015) · low 0 (2018)2026

Most influential descendants

Showing 5 of 20 · See all
  • K171840Stryker Consolidated Operating Room Equipment (CORE) 2 ConsoleStryker Corporation · 2017 · cites it directly8descendants
  • K240662Spine Guidance Software (version 5.0); Xia 3/ Serrato Q Instruments; Everest Q…Stryker Leibinger GmbH & Co KG · 2024 · 2 generations on7descendants
  • K141935Stryker S2 DrillStryker Corporation · 2014 · cites it directly7descendants
  • K152641Pi Drive Plus Motor, ExtenderStryker Corporation · 2015 · 2 generations on6descendants
  • K143320Stryker Elite Attachments, Stryker Heavy Duty (HD) AttachmentsStryker Corp. · 2015 · cites it directly6descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K112593Styker Consolidated Operating Room Equipment (Core) SystemStryker Corporation2012—
+1K171840Stryker Consolidated Operating Room Equipment (CORE) 2 ConsoleStryker Corporation2017—
+2K240662Spine Guidance Software (version 5.0); Xia 3/ Serrato Q Instruments; Everest Q…Stryker Leibinger GmbH & Co KG2024—
+1K141935Stryker S2 DrillStryker Corporation2014—
+2K152641Pi Drive Plus Motor, ExtenderStryker Corporation2015—
+1K143320Stryker Elite Attachments, Stryker Heavy Duty (HD) AttachmentsStryker Corp.20157

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201540
201610
201710
201920
202120
202430
202520
202640
FIG. 1 — Lineage of K112593, 2012–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in ERL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new ERL device

  1. #1 K243280 Piezomed Pro (Piezomed Pro module M-PM100…score 12.0 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (3)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*—Stryker Consolidated Operating Room Equipment (CORE) System
Named without a submission number
—
*—Synthes Electric Pen Drive (EPD) System
Named without a submission number
—
*—Stryker Total Performance System
Named without a submission number
—

What descends from it? (20)

See all 20

6 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K171840Stryker Consolidated Operating Room Equipment (CORE) 2 ConsoleStryker Corporation20178
K141935Stryker S2 DrillStryker Corporation20147
K143320Stryker Elite Attachments, Stryker Heavy Duty (HD) AttachmentsStryker Corp.20156
K241171Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2…Stryker Leibinger GmbH & Co KG20244
K143540Stryker MIS Attachments and Cutting AccessoriesStryker Corporation20154
K143399Stryker Footed Attachments and Cutting AccessoriesStryker Corp.20151

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K171840 (Stryker Corporation, 2017) has gone furthest, with 8 descendants of its own.

How does its category compare?

All ERL devices

ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · ERL

1in 2025

2008: 62009: 12012: 22013: 22014: 12015: 32016: 42017: 22018: 12019: 12020: 12021: 12022: 32024: 12025: 1
2007high 6 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ERL

191in 2022

2008: 181 days median2015: 86 days median2016: 180 days median2022: 191 days median
2007high 191 (2022) · low 86 (2015)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · ERL

1in 2021

2009: 12013: 32020: 52021: 1
2007high 5 (2020) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ERL

1,469in 2025

2007: 1122008: 602009: 2492010: 4442011: 1,0682012: 1,3792013: 3,2312014: 1,9752015: 2,6302016: 1,4552017: 9992018: 1,3802019: 2,5152020: 2,3692021: 2,2832022: 1,5742023: 1,7252024: 1,5882025: 1,469
2007high 3,231 (2013) · low 60 (2008)2025

MAUDE reports naming product code ERL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—0112
20086181060
20091—1249
20100—0444
20110—01,068
20122—01,379
20132—33,231
20141—01,975
201538602,630
2016418001,455
20172—0999
20181—01,380
20191—02,515
20201—52,369
20211—12,283
2022319101,574
20230—01,725
20241—01,588
20251—01,469
20260—0—

What is it indicated for?

The Stryker® Consolidated Operating Room Equipment (CORE) System is intended for use in the cutting, drilling, reaming, decorticating, shaping, and smoothing of bone, bone cement and teeth in a variety of surgical procedures, including but not limited to, dental, ENT (ear, nose, throat), neuro, spine, and endoscopic applications. It is also usable in the placement or cutting of screws, metal, wires, pins, and other fixation devices.

Indications for use as stated in the FDA summary.

More from Stryker Corporation

87 FDA decisions under this applicant name. See the company

  • K232157Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice…Stryker Corporation · 2023
  • K223770Sonopet 1Q 3 7cm 1Q LargeStryker Corporation · 2023
  • K212194Stryker Q Guidance System with Cranial Guidance Software, CranialMask Tracker and Microscope Tracker…Stryker Corporation · 20232 recalls
  • K221728Aviator® Anterior Cervical Plating (ACP) System, LITe® Plate System, DynaTran™ Anterior Cervical Plating…Stryker Corporation · 2022
  • K221074OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion DeviceStryker Corporation · 2022

Recent decisions in ERL

The ERL category page

  • K243280Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips)…W&H Dentalwerk Buermoos GmbH · 2025
  • K233958hekaDrillZethon, Ltd. · 2024
  • K221184ORiGO SystemBien-Air Surgery SA · 2022
  • K213221AMADEO, M-UK1015 (incl. attachments and accessories)W&H Dentalwerk Buermoss GmbH · 2022
  • K212650Celeris, Disposable Sinus DebriderGyrus Acmi, Inc. · 2022

https://510kreport.com/device/K112593 · printed Nov 3, 2026

Cite this page

510(k) Report. “K112593: Styker Consolidated Operating Room Equipment (Core) System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K112593

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026