510(k) Report

510(k) · Cleared

Recalled · 2010

Trilogy System with Rapidarc

K072916510(k) SpecialCleared Nov 9, 200728-day reviewClass II21 CFR 892.5050Recalls 2

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

Varian Medical Systems, Inc. · IYE Accelerator, Linear, Medical

Cleared on Nov 9, 2007 as substantially equivalent to K070094 (Varian Medical Systems, Inc., 2007) after a 28-day review. Its family tree reaches back 4 generations to 1991. 77 later devices descend from it. It has been recalled 2 times.

Decided
Nov 9, 2007
Review
28 days
Class
Class II
Product code
IYE
Recalls
2
Predicates
1

Its longest line of descent runs back 4 generations to K913119 (1991). 6 ancestors in all. 77 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 1 other ancestor2000: 1 other ancestor2009: 3 descendants cleared2008: 1 descendant cleared2012: 3 descendants cleared2010: 2 descendants cleared2011: 3 descendants cleared2013: 4 descendants cleared2024: 3 descendants cleared2014: 4 descendants cleared2017: 7 descendants cleared2018: 7 descendants cleared2016: 3 descendants cleared2019: 5 descendants cleared2015: 3 descendants cleared2022: 4 descendants cleared2021: 7 descendants cleared2026: 5 descendants cleared2023: 9 descendants cleared2025: 2 descendants cleared2020: 2 descendants clearedK913119 · Varian C-Series Clinacs (Clinac 2300C/D) · Varian Assoc., Inc. · 1991 · recalledK033343 · Trilogy Radiotherapy Delivery System · Varian Medical Systems, Inc. · 2003 · recalledK061140 · Trilogy Radiotherapy Delivery System · Varian Medical Systems · 2006K070094 · Trilogy Radiotherapy Delivery System and Trilogy TX Delivery System · Varian Medical Systems, Inc. · 2007 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 2 other ancestors 1 generation forward: 6 descendants2 generations forward: 9 descendants3 generations forward: 7 descendants4 generations forward: 7 descendants5 generations forward: 10 descendants6 generations forward: 8 descendants7 generations forward: 7 descendants8 generations forward: 6 descendants9 generations forward: 5 descendants10 generations forward: 4 descendants11 generations forward: 4 descendants12 generations forward: 3 descendants13 generations forward: 1 descendant K070094 · Trilogy Radiotherapy Delivery System and Trilogy TX Delivery System · Varian Medical Systems, Inc. · 2007 · recalledK061140 · Trilogy Radiotherapy Delivery System · Varian Medical Systems · 2006K033343 · Trilogy Radiotherapy Delivery System · Varian Medical Systems, Inc. · 2003 · recalledK913119 · Varian C-Series Clinacs (Clinac 2300C/D) · Varian Assoc., Inc. · 1991 · recalled0+5+10
  1. Root · 4 generations backK913119 Varian C-Series Clinacs (Clinac 2300C/D)Varian Assoc., Inc. · 1991 · Recalled
  2. 3 generations backK033343 Trilogy Radiotherapy Delivery SystemVarian Medical Systems, Inc. · 2003 · Recalled
  3. 2 generations backK061140 Trilogy Radiotherapy Delivery SystemVarian Medical Systems · 2006
  4. 1 generation backK070094 Trilogy Radiotherapy Delivery System and Trilogy TX Delivery SystemVarian Medical Systems, Inc. · 2007 · Recalled
  5. This deviceK072916 Trilogy System with RapidarcVarian Medical Systems, Inc. · 2007
  6. Descendant · cites it directly · 61 of its ownK092871 Trilogy MXVarian Medical Systems, Inc. · 2009 · Recalled
  7. Descendant · 2 generations on · 43 of its ownK111106 TruebeamVarian Medical Systems, Inc. · 2011 · Recalled
  8. Descendant · 3 generations on · 37 of its ownK123291 TruebeamVarian Medical Systems, Inc. · 2012
  9. Descendant · 3 generations on · 36 of its ownK123808 AgilityElekta, Ltd. · 2013 · Recalled
  10. Descendant · 4 generations on · 31 of its ownK140528 True Beam, True Beam STX, EdgeVarian Medical Systems, Inc. · 2014 · Recalled

Showing 5 of 77 descendants. See all descendants

Descendants cleared per year

2008: 12009: 32010: 22011: 32012: 32013: 42014: 42015: 32016: 32017: 72018: 72019: 52020: 22021: 72022: 42023: 92024: 32025: 22026: 5
2008high 9 (2023) · low 1 (2008)2026

Most influential descendants

Showing 5 of 77 · See all
  • K092871Trilogy MXVarian Medical Systems, Inc. · 2009 · cites it directly61descendants
  • K111106TruebeamVarian Medical Systems, Inc. · 2011 · 2 generations on43descendants
  • K123291TruebeamVarian Medical Systems, Inc. · 2012 · 3 generations on37descendants
  • K123808AgilityElekta, Ltd. · 2013 · 3 generations on36descendants
  • K140528True Beam, True Beam STX, EdgeVarian Medical Systems, Inc. · 2014 · 4 generations on31descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K913119Varian C-Series Clinacs (Clinac 2300C/D)Varian Assoc., Inc.19916
−3K033343Trilogy Radiotherapy Delivery SystemVarian Medical Systems, Inc.20033
−2K061140Trilogy Radiotherapy Delivery SystemVarian Medical Systems2006—
−1K070094Trilogy Radiotherapy Delivery System and Trilogy TX Delivery SystemVarian Medical Systems, Inc.20075
0 (this device)K072916Trilogy System with RapidarcVarian Medical Systems, Inc.2007—
+1K092871Trilogy MXVarian Medical Systems, Inc.20095
+2K111106TruebeamVarian Medical Systems, Inc.20115
+3K123291TruebeamVarian Medical Systems, Inc.2012—
+3K123808AgilityElekta, Ltd.20132
+4K140528True Beam, True Beam STX, EdgeVarian Medical Systems, Inc.20142

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
200930
201020
201130
201230
201340
201440
201530
201630
201770
201870
201950
202020
202170
202240
202390
202430
202520
202650
FIG. 1 — Lineage of K072916, 1991–2026Source: 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 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? (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
*K070094Trilogy Radiotherapy Delivery System and Trilogy TX Delivery System
Summary page 1
…Class II Product Code: 90 IYE 3. Predicate Device to claim substantial equivalence: Varian Trilogy Tx Radiotherapy System -K070094 4. Description of the Device: The Trilogy System modifications enable the delivery a RapidArc treatment field…
Varian Medical Systems, Inc.20075

What descends from it? (77)

See all 77

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

NumberDeviceApplicantDecidedDescendants
K092871Trilogy MXVarian Medical Systems, Inc.200961
K081188Trilogy with External System Gating InterfaceVarian Medical Systems, Inc.20086
K100890Varian High Energy Linear AcceleratorVarian Medical Systems20104
K121295Artistetm Solution with Sys VcioSiemens Medical Solutions USA, Inc.20123
K101751Varian Unique Single Energy Linear AcceleratorVarian Medical Systems, Oncology Systems20103
K090808PINNACLE3 SmartarcPhilips Medical Systems, Inc.20090

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

Recalls of this device

DateClassRecallRoot causeReason
Jul 20, 2010Not classifiedZ-0821-2011Software designThe system may deliver an inaccurate dose that does not match the treatment plan. As a result of a system configuration problem, the VMAT (Volumetric Modulated Arc Therapy) plans may be delivered as Dynamic Arc therapy plans. If this…
Dec 1, 2009Not classifiedZ-1001-2011Device DesignA circuit design anomaly whereby a faulty balance potentiometer can lead to an undetected electron beam asymmetry.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 16 years and passes through 3 companies; a new generation was cleared every 2.4 years on median.
  • 4 of the 6 ancestors have a recall of any class.
  • Of its descendants, K092871 (Varian Medical Systems, Inc., 2009) has gone furthest, with 61 descendants of its own.

How does its category compare?

All IYE devices

IYE Accelerator, Linear, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, 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?

The Trilogy Tm System with RapidArc is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K072916: Trilogy System with Rapidarc.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K072916

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