510(k) Report

510(k) · Cleared

Cleared

Microtable System

K132611510(k) TraditionalCleared Mar 6, 2014198-day reviewClass II21 CFR 882.4560

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

Fred Haer Company, Inc. · HAW Neurological Stereotaxic Instrument

Cleared on Mar 6, 2014 as substantially equivalent to K092192 (FHC, Inc., 2010) after a 198-day review. Its family tree reaches back 3 generations to 1986. 1 later device descends from it.

Decided
Mar 6, 2014
Review
198 days
Class
Class II
Product code
HAW
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K854886 (1986). 9 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2001: 1 other ancestor1998: 1 other ancestor2004: 1 other ancestor1995: 1 other ancestor1990: 1 other ancestor2024: 1 descendant clearedK854886 · Wuerzburg Titanium Mini Bone Plates & Bone Screws · Walter Lorenz Surgical, Inc. · 1986 · recalledK961120 · Marker System for Stereotaxic Navigation · Howmedica Leibinger, Inc. · 1996K092192 · Waypoint Stereotactic System · FHC, Inc. · 20101990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 3 other ancestors3 generations back: 3 other ancestors 1 generation forward: 1 descendant K092192 · Waypoint Stereotactic System · FHC, Inc. · 2010K961120 · Marker System for Stereotaxic Navigation · Howmedica Leibinger, Inc. · 1996K854886 · Wuerzburg Titanium Mini Bone Plates & Bone Screws · Walter Lorenz Surgical, Inc. · 1986 · recalled0
  1. Root · 3 generations backK854886 Wuerzburg Titanium Mini Bone Plates & Bone ScrewsWalter Lorenz Surgical, Inc. · 1986 · Recalled
  2. 2 generations backK961120 Marker System for Stereotaxic NavigationHowmedica Leibinger, Inc. · 1996
  3. 1 generation backK092192 Waypoint Stereotactic SystemFHC, Inc. · 2010
  4. This deviceK132611 Microtable SystemFred Haer Company, Inc. · 2014
  5. Descendant · cites it directly · 0 of its ownK233703 Bone Anchor (NGS-BA-01)ClearPoint Neuro, Inc. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K233703Bone Anchor (NGS-BA-01)ClearPoint Neuro, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K854886Wuerzburg Titanium Mini Bone Plates & Bone ScrewsWalter Lorenz Surgical, Inc.19861
−2K961120Marker System for Stereotaxic NavigationHowmedica Leibinger, Inc.1996—
−1K092192Waypoint Stereotactic SystemFHC, Inc.2010—
0 (this device)K132611Microtable SystemFred Haer Company, Inc.2014—
+1K233703Bone Anchor (NGS-BA-01)ClearPoint Neuro, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199510
199810
200110
200410
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K132611, 1986–2024Source: 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 HAW? 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 HAW device

  1. #1 K253856 Geniant Cranial (Navigated Neurosurgical…score 15.0 · 11 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? (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
*K092192Waypoint Stereotactic System
Summary page 1
…vice to which the submitter claims substantial equivalence: The Microtable System is substantially equivalent to FHC, Inc.'s WayPoint TM Stereotactic System (K092192; decision date: February 12, 2010: product code HAW). (4) Description of device: The Microtable System is a patient-speci…
FHC, Inc.2010—

Also cleared against K092192: 2 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
K233703Bone Anchor (NGS-BA-01)ClearPoint Neuro, Inc.20240

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 28 years and passes through 4 companies; a new generation was cleared every 10.3 years on median.
  • 3 of the 9 ancestors have a recall of any class.
  • Of its descendants, K233703 (ClearPoint Neuro, Inc., 2024) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K092192.

How does its category compare?

All HAW devices

HAW Neurological Stereotaxic Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · HAW

9in 2025

2007: 152008: 122009: 82010: 62011: 42012: 82013: 32014: 52015: 102016: 92017: 72018: 62019: 102020: 52021: 92022: 72023: 142024: 72025: 92026 (partial year): 5
2007high 15 (2007) · low 3 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HAW

163in 2025

2007: 107 days median2008: 112 days median2009: 221 days median2010: 138 days median2011: 66 days median2012: 178 days median2013: 172 days median2014: 238 days median2015: 232 days median2016: 175 days median2017: 226 days median2018: 112 days median2019: 147 days median2020: 88 days median2021: 168 days median2022: 128 days median2023: 142 days median2024: 107 days median2025: 163 days median2026 (partial year): 162 days median
2007high 238 (2014) · low 66 (2011)2026

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

Recalls per year · HAW

2in 2025

2007: 22008: 102009: 62010: 282011: 52012: 42013: 6, 1 Class I2014: 52015: 32016: 52017: 22018: 2, 2 Class I2019: 4, 1 Class I2020: 12021: 4, 2 Class I2022: 12023: 4, 1 Class I2024: 2, 2 Class I2025: 22026 (partial year): 6
2007high 28 (2010) · low 1 (2020)2026

Class I (9 since 2007) Class II/III not classified

Adverse event reports per year · HAW

3,425in 2025

2007: 492008: 532009: 962010: 2992011: 1,7252012: 9862013: 1,2902014: 1,6062015: 1,7672016: 1,8282017: 3,5052018: 4,4392019: 6,0622020: 3,4802021: 2,8272022: 1,9292023: 2,5102024: 3,7552025: 3,425
2007high 6,062 (2019) · low 49 (2007)2025

MAUDE reports naming product code HAW, 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
200715107249
2008121121053
20098221696
2010613828299
201146651,725
201281784986
201331726 (1)1,290
2014523851,606
20151023231,767
2016917551,828
2017722623,505
201861122 (2)4,439
2019101474 (1)6,062
202058813,480
202191684 (2)2,827
2022712811,929
2023141424 (1)2,510
202471072 (2)3,755
2025916323,425
202651626—

What is it indicated for?

The Microtable System is intended to be used with commercially available stereotactic systems for intra-cranial and neurosurgical procedures which require the accurate positioning of microelectrodes, stimulating electrodes, or other instruments in the cranium, brain, or nervous system.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K132611: Microtable System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132611

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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