510(k) Report

510(k) · Cleared

Cleared

Patient Positioning Devices

K142420510(k) TraditionalCleared Mar 27, 2015211-day reviewClass II21 CFR 892.5050

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

Macromedics BV · IYE Accelerator, Linear, Medical

Cleared on Mar 27, 2015 as substantially equivalent to K060737 (Sinmed BV, 2006) and 2 other predicates after a 211-day review. Its family tree reaches back 5 generations to 1991. 7 later devices descend from it.

Decided
Mar 27, 2015
Review
211 days
Class
Class II
Product code
IYE
Recalls
None
Predicates
3

Its longest line of descent runs back 5 generations to K905007 (1991). 17 ancestors in all. 7 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2002: 1 other ancestor1998: 2 other ancestors1997: 1 other ancestor1995: 3 other ancestors1994: 3 other ancestors1993: 1 other ancestor2022: 2 descendants cleared2023: 2 descendants cleared2021: 1 descendant cleared2020: 1 descendant cleared2025: 1 descendant clearedReference device: K093738 · Mri Patient Positioning Devices · Medtec, Inc. · 2010Reference device: K121545 · Bellyboard, SBRT Accessories · Medtec Inc. Dba Civco Medical Solutions · 2012 · recalledK905007 · Standard Breast Boards; Deluxe Breast Board · Bionix Development Corp. · 1991K030051 · Versaboard, Model 7040 · Bionix Development Corp. · 2003K060737 · Sinmed Positioning Devices · Sinmed BV · 2006K093738 · Mri Patient Positioning Devices · Medtec, Inc. · 2010K111340 · Head and Neck Immobilization System, Body Immobilization System · Medtec, Inc. · 20111990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 11 other ancestors 1 generation forward: 5 descendants2 generations forward: 2 descendants K111340 · Head and Neck Immobilization System, Body Immobilization System · Medtec, Inc. · 2011K093738 · Mri Patient Positioning Devices · Medtec, Inc. · 2010K060737 · Sinmed Positioning Devices · Sinmed BV · 2006K030051 · Versaboard, Model 7040 · Bionix Development Corp. · 2003K905007 · Standard Breast Boards; Deluxe Breast Board · Bionix Development Corp. · 1991−50
  1. Root · 5 generations backK905007 Standard Breast Boards; Deluxe Breast BoardBionix Development Corp. · 1991
  2. 4 generations backK030051 Versaboard, Model 7040Bionix Development Corp. · 2003
  3. 3 generations backK060737 Sinmed Positioning DevicesSinmed BV · 2006
  4. 2 generations backK093738 Mri Patient Positioning DevicesMedtec, Inc. · 2010
  5. 1 generation backK111340 Head and Neck Immobilization System, Body Immobilization SystemMedtec, Inc. · 2011
  6. This deviceK142420 Patient Positioning DevicesMacromedics BV · 2015
  7. Descendant · cites it directly · 2 of its ownK212909 VacuumCushions, FeetSupports, LEPS (Lower Extermities Positioning…Macromedics BV · 2022
  8. Descendant · cites it directly · 1 of its ownK222977 DSPS-Prominent™ Masks; DSPS-Prominent™ Baseplate, MR; CouchStripMacromedics BV · 2023
  9. Descendant · cites it directly · 1 of its ownK210894 Siddharth-II; ImpactPanacea Medical Technologies Pvt., Ltd. · 2021
  10. Descendant · 2 generations on · 0 of its ownK250429 DSPS-Prominent® baseplate, MR (113820); DSPS-Prominent® baseplate…Macromedics BV · 2025
  11. Descendant · 2 generations on · 0 of its ownK222762 Siddharth-II;ImpactPanacea Medical Technologies Pvt., Ltd. · 2023

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2020: 12021: 12022: 22023: 22025: 1
2020high 2 (2022) · low 0 (2024)2026

Most influential descendants

Showing 5 of 7 · See all
  • K212909VacuumCushions, FeetSupports, LEPS (Lower Extermities Positioning System), CouchStripsMacromedics BV · 2022 · cites it directly2descendants
  • K222977DSPS-Prominent™ Masks; DSPS-Prominent™ Baseplate, MR; CouchStripMacromedics BV · 2023 · cites it directly1descendant
  • K210894Siddharth-II; ImpactPanacea Medical Technologies Pvt., Ltd. · 2021 · cites it directly1descendant
  • K250429DSPS-Prominent® baseplate, MR (113820); DSPS-Prominent® baseplate (113120)…Macromedics BV · 2025 · 2 generations on0descendants
  • K222762Siddharth-II;ImpactPanacea Medical Technologies Pvt., Ltd. · 2023 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K905007Standard Breast Boards; Deluxe Breast BoardBionix Development Corp.1991—
−4K030051Versaboard, Model 7040Bionix Development Corp.2003—
−3K060737Sinmed Positioning DevicesSinmed BV2006—
−2K093738Mri Patient Positioning DevicesMedtec, Inc.2010—
−1K111340Head and Neck Immobilization System, Body Immobilization SystemMedtec, Inc.2011—
0 (this device)K142420Patient Positioning DevicesMacromedics BV2015—
+1K212909VacuumCushions, FeetSupports, LEPS (Lower Extermities Positioning System)…Macromedics BV2022—
+1K222977DSPS-Prominent™ Masks; DSPS-Prominent™ Baseplate, MR; CouchStripMacromedics BV2023—
+1K210894Siddharth-II; ImpactPanacea Medical Technologies Pvt., Ltd.2021—
+2K250429DSPS-Prominent® baseplate, MR (113820); DSPS-Prominent® baseplate (113120)…Macromedics BV2025—
+2K222762Siddharth-II;ImpactPanacea Medical Technologies Pvt., Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199430
199530
199710
199820
200210
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
202220
202320
202510
FIG. 1 — Lineage of K142420, 1991–2025Source: 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 IYE? 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 IYE device

  1. #1 K252977 Halcyon, Ethos Radiotherapy System (5.0)score 18.8 · 18 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
*K060737Sinmed Positioning Devices
Summary page 5
…g environment. MacroMedics devices Predicate devices: 510(k) number: ExaFix-5 Sinmed Posifix-2 K060737 (IYE) ExaFix-5A Sinmed Posifix-1 K060737 (IYE)…
Sinmed BV2006—
*K111340Head and Neck Immobilization System, Body Immobilization System
Summary page 11
…MR safe. MacroMedics Devices Predicate devices: 510(k) number: SBRT EAMIS CIVCO Body Pro Lok K111340 (LNH & IYE) SBRT OmniBoard (UATB) CIVCO Body Pro Lok K111340 (LNH & IYE) SBRT MultiBoard (UT…
Medtec, Inc.2011—
*K080072Mri Patient Positioning Devices
Summary page 13
…nd profiles immobilization system K093738 (LNH, reference device) DSPS & SSPS thermoplastic CIVCO head K080072 (IYE) masks immobilization plastics K093738 (LNH, reference device) DSPS & SSPS c…
CIVCO Medical Instruments Co., Inc.2008—
†K093738Mri Patient Positioning DevicesMedtec, Inc.2010—
†K121545Bellyboard, SBRT AccessoriesMedtec Inc. Dba Civco Medical Solutions20122

Also cleared against K060737: 3 other devices →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K212909VacuumCushions, FeetSupports, LEPS (Lower Extermities Positioning System), CouchStripsMacromedics BV20222
K222977DSPS-Prominent™ Masks; DSPS-Prominent™ Baseplate, MR; CouchStripMacromedics BV20231
K210894Siddharth-II; ImpactPanacea Medical Technologies Pvt., Ltd.20211
K213439FlexBoardTM, EagleBoardTM, BreastBoard SXTMMacromedics BV20220
K193243Alta Multipurpose DeviceQfix20200

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 24 years and passes through 4 companies; a new generation was cleared every 3.7 years on median.
  • 2 of the 17 ancestors have a recall of any class.
  • Of its descendants, K212909 (Macromedics BV, 2022) has gone furthest, with 2 descendants of its own.
  • 3 other devices also cite its predicate K060737.

How does its category compare?

All IYE devices

IYE Accelerator, Linear, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · IYE

12in 2025

2007: 232008: 142009: 202010: 232011: 112012: 282013: 182014: 202015: 202016: 212017: 232018: 212019: 192020: 202021: 192022: 122023: 182024: 92025: 122026 (partial year): 14
2007high 28 (2012) · low 9 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYE

170in 2025

2007: 44 days median2008: 69 days median2009: 63 days median2010: 74 days median2011: 94 days median2012: 106 days median2013: 88 days median2014: 100 days median2015: 108 days median2016: 97 days median2017: 94 days median2018: 58 days median2019: 83 days median2020: 67 days median2021: 86 days median2022: 172 days median2023: 129 days median2024: 239 days median2025: 170 days median2026 (partial year): 120 days median
2007high 239 (2024) · low 44 (2007)2026

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

Recalls per year · IYE

1in 2025

2007: 782008: 492009: 222010: 272011: 732012: 202013: 112014: 142015: 82016: 72017: 72018: 72019: 22020: 42021: 52022: 32023: 72024: 12025: 12026 (partial year): 4
2007high 78 (2007) · low 1 (2024)2026

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

Adverse event reports per year · IYE

101in 2025

2007: 1552008: 1142009: 1742010: 2462011: 2802012: 1282013: 962014: 1242015: 1002016: 972017: 1252018: 852019: 912020: 742021: 682022: 662023: 1282024: 812025: 101
2007high 280 (2011) · low 66 (2022)2025

MAUDE reports naming product code IYE, 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
2007234478155
2008146949114
2009206322174
2010237427246
2011119473280
20122810620128
201318881196
20142010014124
2015201088100
20162197797
201723947125
20182158785
20191983291
20202067474
20211986568
202212172366
2023181297128
20249239181
2025121701101
2026141204—

What is it indicated for?

Positioning of the patient during radiotherapy and radio diagnostics, including MR where indicated.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K142420: Patient Positioning Devices.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142420

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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