510(k) Report

510(k) · Cleared

Recalled · Class II · 2021

Electric Drill System [XPS 4000 System, Midas Rex Legend Ehs System, Integrated Power Console (Ipc)]

K081475510(k) TraditionalCleared Oct 17, 2008143-day reviewClass II21 CFR 882.4310Recalls 3

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

Medtronic Xomed, Inc. · HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)

Cleared on Oct 17, 2008 as substantially equivalent to K073255 (Medtronic Xomed, Inc., 2008) and 5 other predicates after a 143-day review. Its family tree reaches back 6 generations to 1986. 1 of the 470 devices in its family, counting itself, has a Class I recall. 443 later devices descend from it. It has been recalled 3 times.

Decided
Oct 17, 2008
Review
143 days
Class
Class II
Product code
HBE
Recalls
3
Predicates
6

Its longest line of descent runs back 6 generations to K862807 (1986). 26 ancestors in all, the oldest K852143 (1985). 443 later devices descend from it, 11 citing it directly. 1 of the 470 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2001: 2 other ancestors2000: 2 other ancestors1994: 4 other ancestors2004: 2 other ancestors1995: 5 other ancestors1998: 1 other ancestor1986: 1 other ancestor1996: 1 other ancestor1985: 1 other ancestor2024: 64 descendants cleared2014: 3 descendants cleared2012: 1 descendant cleared2013: 5 descendants cleared2021: 43 descendants cleared, 1 with a Class I recall12017: 15 descendants cleared2016: 8 descendants cleared2011: 1 descendant cleared2015: 6 descendants cleared2018: 17 descendants cleared2020: 23 descendants cleared2023: 63 descendants cleared2022: 47 descendants cleared2019: 26 descendants cleared2026: 56 descendants cleared2025: 65 descendants clearedK862807 · Treace Drill System · Treace Medical, Inc. · 1986×2: 2 generations cleared close together, K964548 (1997), K971059 (1997) K981637 · Integrated Drive/Pump System for Otolaryngology · Linvatec Corp. · 1998K990524 · E9000 System · Linvatec Corp. · 1999K012456 · Sodem High Speed System (Electric) (Ear, Nose, and Throat) · Sodemsystems · 20011990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 5 other ancestors2 generations back: 6 other ancestors3 generations back: 2 other ancestors4 generations back: 5 other ancestors5 generations back: 2 other ancestors 1 generation forward: 11 descendants2 generations forward: 22 descendants3 generations forward: 112 descendants4 generations forward: 113 descendants5 generations forward: 67 descendants6 generations forward: 55 descendants, 1 with a Class I recall17 generations forward: 24 descendants8 generations forward: 23 descendants9 generations forward: 12 descendants10 generations forward: 3 descendants11 generations forward: 1 descendant K012456 · Sodem High Speed System (Electric) (Ear, Nose, and Throat) · Sodemsystems · 2001K990524 · E9000 System · Linvatec Corp. · 1999K981637 · Integrated Drive/Pump System for Otolaryngology · Linvatec Corp. · 1998K971059 · Universal Drive System · Linvatec Corp. · 1997K964548 · Apex Universal Drive System · Linvatec Corp. · 1997K862807 · Treace Drill System · Treace Medical, Inc. · 1986−50+5+10
  1. Root · 6 generations backK862807 Treace Drill SystemTreace Medical, Inc. · 1986
  2. 5 generations backK964548 Apex Universal Drive SystemLinvatec Corp. · 1997
  3. 4 generations backK971059 Universal Drive SystemLinvatec Corp. · 1997
  4. 3 generations backK981637 Integrated Drive/Pump System for OtolaryngologyLinvatec Corp. · 1998
  5. 2 generations backK990524 E9000 SystemLinvatec Corp. · 1999
  6. 1 generation backK012456 Sodem High Speed System (Electric) (Ear, Nose, and Throat)Sodemsystems · 2001
  7. This deviceK081475 Electric Drill System [XPS 4000 System, Midas Rex Legend Ehs System…Medtronic Xomed, Inc. · 2008
  8. Descendant · cites it directly · 418 of its ownK111520 Ipc Powerease SystemMedtronic Xomed, Inc. · 2011 · Recalled
  9. Descendant · 2 generations on · 404 of its ownK124004 Navigated CD Horizon Solera Screwdrivers, Taps, Iliac Taps, Legacy…Medtronic Navigation, Inc. · 2013 · Recalled
  10. Descendant · 2 generations on · 398 of its ownK123270 Powerease SystemMedtronic Sofamor Danek USA, Inc. · 2013
  11. Descendant · 2 generations on · 396 of its ownK140454 Navigated CD Horizon Solera Screwdriver/TapsMedtronic Sofamor Danek USA, Inc. · 2014 · Recalled
  12. Descendant · 3 generations on · 246 of its ownK131425 Navigated Capstone Trials, Clydesdale Trials, Capstone & Clydesdale…Medtronic Navigation, Inc. · 2013 · Recalled

Showing 5 of 443 descendants. See all descendants

Descendants cleared per year

2011: 12012: 12013: 52014: 32015: 62016: 82017: 152018: 172019: 262020: 232021: 432022: 472023: 632024: 642025: 652026: 56
2011high 65 (2025) · low 1 (2011)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 443 · See all
  • K111520Ipc Powerease SystemMedtronic Xomed, Inc. · 2011 · cites it directly418descendants
  • K124004Navigated CD Horizon Solera Screwdrivers, Taps, Iliac Taps, Legacy TapsMedtronic Navigation, Inc. · 2013 · 2 generations on404descendants
  • K123270Powerease SystemMedtronic Sofamor Danek USA, Inc. · 2013 · 2 generations on398descendants
  • K140454Navigated CD Horizon Solera Screwdriver/TapsMedtronic Sofamor Danek USA, Inc. · 2014 · 2 generations on396descendants
  • K131425Navigated Capstone Trials, Clydesdale Trials, Capstone & Clydesdale InserterMedtronic Navigation, Inc. · 2013 · 3 generations on246descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K862807Treace Drill SystemTreace Medical, Inc.1986—
−5K964548Apex Universal Drive SystemLinvatec Corp.1997—
−4K971059Universal Drive SystemLinvatec Corp.1997—
−3K981637Integrated Drive/Pump System for OtolaryngologyLinvatec Corp.1998—
−2K990524E9000 SystemLinvatec Corp.1999—
−1K012456Sodem High Speed System (Electric) (Ear, Nose, and Throat)Sodemsystems2001—
0 (this device)K081475Electric Drill System [XPS 4000 System, Midas Rex Legend Ehs System…Medtronic Xomed, Inc.2008—
+1K111520Ipc Powerease SystemMedtronic Xomed, Inc.20112
+2K124004Navigated CD Horizon Solera Screwdrivers, Taps, Iliac Taps, Legacy TapsMedtronic Navigation, Inc.20131
+2K123270Powerease SystemMedtronic Sofamor Danek USA, Inc.2013—
+2K140454Navigated CD Horizon Solera Screwdriver/TapsMedtronic Sofamor Danek USA, Inc.20141
+3K131425Navigated Capstone Trials, Clydesdale Trials, Capstone & Clydesdale InserterMedtronic Navigation, Inc.201310

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198610
199440
199550
199610
199810
200020
200120
200420
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201350
201430
201560
201680
2017150
2018170
2019260
2020230
2021431
2022470
2023630
2024640
2025650
2026560
FIG. 1 — Lineage of K081475, 1986–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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.

1 device in this family has a Class I recall. 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 HBE device

  1. #1 K251433 Surgify Halo (54.085.SHD.H1); Surgify Halo…score 13.2 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (6)

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
*K073255XPS 3000 System
Summary page 1
…(21 CFR 882.4310, Product Code HBE, Class II) Marketed device claiming equivalence to The electric drill system is equivalent to the Medtronic Xomed XPS system K073255, the Midas Rex Legend EHS system (K935567, K012453, K012456, K012457), and to the Linvatec Advantage Drive Electric System (K0025…
Medtronic Xomed, Inc.2008—
*K935567Sodem Power System
Summary page 1
…E, Class II) Marketed device claiming equivalence to The electric drill system is equivalent to the Medtronic Xomed XPS system K073255, the Midas Rex Legend EHS system (K935567, K012453, K012456, K012457), and to the Linvatec Advantage Drive Electric System (K002523). Device Description The electric dril…
Sodemsystems1994—
*K012453Sodem High Speed System (Electric) (General Orthopedics & Plastic Surgery)
Summary page 1
…II) Marketed device claiming equivalence to The electric drill system is equivalent to the Medtronic Xomed XPS system K073255, the Midas Rex Legend EHS system (K935567, K012453, K012456, K012457), and to the Linvatec Advantage Drive Electric System (K002523). Device Description The electric drill system…
Sodemsystems2001—
*K012456Sodem High Speed System (Electric) (Ear, Nose, and Throat)
Summary page 1
…eted device claiming equivalence to The electric drill system is equivalent to the Medtronic Xomed XPS system K073255, the Midas Rex Legend EHS system (K935567, K012453, K012456, K012457), and to the Linvatec Advantage Drive Electric System (K002523). Device Description The electric drill system consists…
Sodemsystems2001—
*K012457Sodem High Speed System (Electric) (Neuro/Spine Surgery)
Summary page 1
…ce claiming equivalence to The electric drill system is equivalent to the Medtronic Xomed XPS system K073255, the Midas Rex Legend EHS system (K935567, K012453, K012456, K012457), and to the Linvatec Advantage Drive Electric System (K002523). Device Description The electric drill system consists of a powe…
Sodemsystems2001—
*K002523Advantage Drive System
Summary page 1
…ent to the Medtronic Xomed XPS system K073255, the Midas Rex Legend EHS system (K935567, K012453, K012456, K012457), and to the Linvatec Advantage Drive Electric System (K002523). Device Description The electric drill system consists of a power console, footswitches, connection cables, irrigation / coolin…
Linvatec Corp.2000—

Also cleared against K073255: 2 other devices →

What descends from it? (443)

See all 443

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

NumberDeviceApplicantDecidedDescendants
K111520Ipc Powerease SystemMedtronic Xomed, Inc.2011418
K121264Triton Electric High Torque Handpiece and Software ModuleMedtronic Surgical Technologies201212
K170312IPC systems, Legend EHS handpieces and Legend Stylus Touch handpiece, Microsaw…Medtronic Powered Surgical Solutions201711
K160713Stealth-Midas SystemMedtronic Powered Surgical Solutions20169
K141122Harmonic Scallop Blade, Generator G11Ethicon Endo-Surgery, LLC20149
K163565MR8 Drill SystemMedtronic Powered Surgical Solutions20177
K132264PRIMADO2 Total Surgical SystemNakanishi, Inc.20136
K130755Hicut Highspeed InstrumentAdeor Medical AG20144
K233958hekaDrillZethon, Ltd.20240
K193630hekaDrillZethon, Ltd.20210

Has anything in its family been recalled? (1 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Dec 15, 2021Class IIZ-0961-2022Under Investigation by firmAs a result of Medtronic's integrated power console (authentication number: 222ACBZX00018000) being used with software version: v2.7.3.0, it was discovered that there was a defect that resulted in a difference between the set number of…
Aug 31, 2021Class IIZ-0158-2022Process controlThere was an increase in complaints related to tip breaks and wobble/vibration.
May 13, 2016Class IIZ-2085-2016Device DesignMedtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm Seal identified a potential for leakage of fluid into the motor during use.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K211616ExcelsiusHubGlobus Medical, Inc. · 2021 · 6 generations on · ◆ in the 2021 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 22 years and passes through 4 companies; a new generation was cleared every 2.2 years on median.
  • 2 of the 26 ancestors have a recall of any class.
  • Of its descendants, K111520 (Medtronic Xomed, Inc., 2011) has gone furthest, with 418 descendants of its own.
  • 2 other devices also cite its predicate K073255.

How does its category compare?

All HBE devices

HBE Drills, Burrs, Trephines & Accessories (Simple, Powered): FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · HBE

6in 2025

2007: 22008: 22011: 22012: 12013: 12014: 22015: 32016: 22017: 22018: 22019: 52021: 62022: 22023: 22025: 62026 (partial year): 1
2007high 6 (2021) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HBE

30in 2025

2015: 155 days median2019: 133 days median2021: 193 days median2025: 30 days median
2007high 193 (2021) · low 30 (2025)2026

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

Recalls per year · HBE

1in 2024

2008: 472009: 72010: 232011: 12012: 262013: 42016: 72017: 32021: 12023: 32024: 12026 (partial year): 19
2007high 47 (2008) · low 0 (2007)2026

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

Adverse event reports per year · HBE

1,924in 2025

2007: 142008: 142009: 2422010: 4922011: 1,0132012: 1,1462013: 1,5832014: 5592015: 4832016: 8482017: 8482018: 7872019: 8362020: 1,0252021: 1,0472022: 9002023: 9482024: 1,1532025: 1,924
2007high 1,924 (2025) · low 14 (2007)2025

MAUDE reports naming product code HBE, 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
20072—014
20082—4714
20090—7242
20100—23492
20112—11,013
20121—261,146
20131—41,583
20142—0559
201531550483
20162—7848
20172—3848
20182—0787
201951330836
20200—01,025
2021619311,047
20222—0900
20232—3948
20240—11,153
202563001,924
20261—19—

What is it indicated for?

The Electric Drill System is indicated for the incision / cutting, removal, drilling, and sawing of soft and hard tissue and bone, and biomaterials in Neurosurgical (Cranial, Craniofacial), Orthopedic, Arthroscopic, Spinal, Sternotomy, and General Surgical Procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K081475: Electric Drill System [XPS 4000 System, Midas Rex Legend Ehs System, Integrated Power Console (Ipc)].” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K081475

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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