510(k) Report

510(k) · Cleared

Cleared

ELAN 4 Electro Motor System Tools

K172709510(k) TraditionalCleared Oct 17, 2018404-day reviewClass II21 CFR 882.4310

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

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

Cleared on Oct 17, 2018 as substantially equivalent to K113476 (The Anspach Effort, Inc., 2011) after a 404-day review. Its family tree reaches back 3 generations to 2001. 1 later device descends from it.

Decided
Oct 17, 2018
Review
404 days
Class
Class II
Product code
HBE
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K011444 (2001). 4 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 3 generations backK011444 Anspach Emax Drill SystemThe Anspach Effort, Inc. · 2001 · Recalled
  2. 2 generations backK080802 Emax 2 Plus System, Model Emax 2 Plus Motor, Emax 2 Console>Firmware…The Anspach Effort, Inc. · 2008 · Recalled
  3. 1 generation backK113476 Anspach Dissection ToolsThe Anspach Effort, Inc. · 2011 · Recalled
  4. This deviceK172709 ELAN 4 Electro Motor System ToolsAesculap, Inc. · 2018
  5. Descendant · cites it directly · 0 of its ownK183203 ELAN 4 ToolsAesculap, Inc. · 2019

Most influential descendants

Showing 1 of 1 · See all
  • K183203ELAN 4 ToolsAesculap, Inc. · 2019 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K011444Anspach Emax Drill SystemThe Anspach Effort, Inc.200170
−2K080802Emax 2 Plus System, Model Emax 2 Plus Motor, Emax 2 Console>Firmware Upgrade…The Anspach Effort, Inc.200835
−1K113476Anspach Dissection ToolsThe Anspach Effort, Inc.201139
0 (this device)K172709ELAN 4 Electro Motor System ToolsAesculap, Inc.2018—
+1K183203ELAN 4 ToolsAesculap, Inc.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
FIG. 1 — Lineage of K172709, 2001–2019Source: 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.

Planning a device in HBE? 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? (1)

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
*K113476Anspach Dissection Tools
Summary page 4
…: 882.4310 PRODUCT CODE: HBE SUBSTANTIAL EQUIVALENCE The ELAN 4 Tools are substantially equivalent to the primary predicate, Anspach Dissection Tools (K113476) and the reference predicate, Aesculap ELAN 4 Electro Motor System (K152960). DEVICE DESCRIPTION The ELAN 4 Tools are cutting de…
The Anspach Effort, Inc.201139
†K152960ELAN 4 Motor SystemAesculap, Inc.2016—

Also cleared against K113476: 5 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K183203ELAN 4 ToolsAesculap, Inc.20190

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?

  • The line of descent spans 17 years and passes through 2 companies; a new generation was cleared every 6.7 years on median.
  • 4 of the 4 ancestors have a recall of any class.
  • Of its descendants, K183203 (Aesculap, Inc., 2019) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K113476.

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. 2018, 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?

Aesculap ELAN 4 Tools are intended for high speed cutting, sawing, and drilling of bone in the fields of Spine, ENT, Neuro, and Maxillofacial Surgery

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K172709: ELAN 4 Electro Motor System Tools.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172709

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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