510(k) Report

510(k) · Cleared

Cleared

Modification to Syngo Inspace 4D

K062673510(k) SpecialCleared Sep 22, 200614-day reviewClass II21 CFR 892.1750

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

Siemens AG Medical Solutions · JAK System, X-Ray, Tomography, Computed

Cleared on Sep 22, 2006 as substantially equivalent to K043469 (Siemens AG Medical Solutions, 2005) after a 14-day review. Its family tree reaches back 5 generations to 1995. 1 of the 181 devices in its family, counting itself, has a Class I recall. 172 later devices descend from it.

Decided
Sep 22, 2006
Review
14 days
Class
Class II
Product code
JAK
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K954355 (1995). 8 ancestors in all. 172 later devices descend from it, 3 citing it directly. 1 of the 181 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1998: 2 other ancestors2008: 1 descendant cleared2011: 3 descendants cleared2012: 6 descendants cleared2010: 1 descendant cleared2009: 1 descendant cleared2014: 8 descendants cleared2015: 7 descendants cleared2016: 8 descendants cleared2019: 12 descendants cleared2013: 3 descendants cleared2020: 18 descendants cleared2018: 11 descendants cleared2017: 7 descendants cleared2025: 17 descendants cleared, 1 with a Class I recall12022: 16 descendants cleared2026: 15 descendants cleared2021: 7 descendants cleared2023: 16 descendants cleared2024: 15 descendants clearedK954355 · Advantage Windows 3D with Navigator Option · General Electric Co. · 1995K974715 · Advantage 3D XR · GE Medical Systems · 1998K984634 · 3D-Angio · Siemens Medical Corp. · 1999K011447 · IN Space 3D · Siemens Medical Solutions USA, Inc. · 2001K043469 · Syngo Inspace 4D · Siemens AG Medical Solutions · 20051995200020052010201520202025
Other ancestors, by generationDescendants, by generation 3 generations back: 2 other ancestors4 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 3 descendants3 generations forward: 15 descendants4 generations forward: 25 descendants5 generations forward: 22 descendants6 generations forward: 21 descendants7 generations forward: 24 descendants, 1 with a Class I recall18 generations forward: 18 descendants9 generations forward: 15 descendants10 generations forward: 7 descendants11 generations forward: 11 descendants12 generations forward: 4 descendants13 generations forward: 2 descendants14 generations forward: 1 descendant15 generations forward: 1 descendant K043469 · Syngo Inspace 4D · Siemens AG Medical Solutions · 2005K011447 · IN Space 3D · Siemens Medical Solutions USA, Inc. · 2001K984634 · 3D-Angio · Siemens Medical Corp. · 1999K974715 · Advantage 3D XR · GE Medical Systems · 1998K954355 · Advantage Windows 3D with Navigator Option · General Electric Co. · 1995−50+5+10+15
  1. Root · 5 generations backK954355 Advantage Windows 3D with Navigator OptionGeneral Electric Co. · 1995
  2. 4 generations backK974715 Advantage 3D XRGE Medical Systems · 1998
  3. 3 generations backK984634 3D-AngioSiemens Medical Corp. · 1999
  4. 2 generations backK011447 IN Space 3DSiemens Medical Solutions USA, Inc. · 2001
  5. 1 generation backK043469 Syngo Inspace 4DSiemens AG Medical Solutions · 2005
  6. This deviceK062673 Modification to Syngo Inspace 4DSiemens AG Medical Solutions · 2006
  7. Descendant · cites it directly · 168 of its ownK073003 Syngo Dual Energy with Extended FunctionallySiemens Medi Cal Solutions, Inc. · 2008
  8. Descendant · 2 generations on · 117 of its ownK083524 Syngo Dual Energy with Extended FunationallySiemens Medical Solutions USA, Inc. · 2009
  9. Descendant · 3 generations on · 99 of its ownK112020 Syngo.CT Vascular AnalysisSiemens Medi Cal Solutions, Inc. · 2011
  10. Descendant · 4 generations on · 63 of its ownK123920 Syngo.ViaSiemens AG Medical Solutions · 2013
  11. Descendant · 2 generations on · 54 of its ownK093621 Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc. · 2010

Showing 5 of 172 descendants. See all descendants

Descendants cleared per year

2008: 12009: 12010: 12011: 32012: 62013: 32014: 82015: 72016: 82017: 72018: 112019: 122020: 182021: 72022: 162023: 162024: 152025: 172026: 15
2008high 18 (2020) · low 1 (2008)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 172 · See all
  • K073003Syngo Dual Energy with Extended FunctionallySiemens Medi Cal Solutions, Inc. · 2008 · cites it directly168descendants
  • K083524Syngo Dual Energy with Extended FunationallySiemens Medical Solutions USA, Inc. · 2009 · 2 generations on117descendants
  • K112020Syngo.CT Vascular AnalysisSiemens Medi Cal Solutions, Inc. · 2011 · 3 generations on99descendants
  • K123920Syngo.ViaSiemens AG Medical Solutions · 2013 · 4 generations on63descendants
  • K093621Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc. · 2010 · 2 generations on54descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K954355Advantage Windows 3D with Navigator OptionGeneral Electric Co.1995—
−4K974715Advantage 3D XRGE Medical Systems1998—
−3K9846343D-AngioSiemens Medical Corp.1999—
−2K011447IN Space 3DSiemens Medical Solutions USA, Inc.2001—
−1K043469Syngo Inspace 4DSiemens AG Medical Solutions2005—
0 (this device)K062673Modification to Syngo Inspace 4DSiemens AG Medical Solutions2006—
+1K073003Syngo Dual Energy with Extended FunctionallySiemens Medi Cal Solutions, Inc.2008—
+2K083524Syngo Dual Energy with Extended FunationallySiemens Medical Solutions USA, Inc.2009—
+3K112020Syngo.CT Vascular AnalysisSiemens Medi Cal Solutions, Inc.2011—
+4K123920Syngo.ViaSiemens AG Medical Solutions2013—
+2K093621Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc.2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199820
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
200910
201010
201130
201260
201330
201480
201570
201680
201770
2018110
2019120
2020180
202170
2022160
2023160
2024150
2025171
2026150
FIG. 1 — Lineage of K062673, 1995–2026Source: 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 JAK device

  1. #1 K230223 iCAC Devicescore 23.5 · 12 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
*K043469Syngo Inspace 4D
Summary page 2
…available software package: Manufacturer Product 510(k) Clearance date Siemens InSpace 4D K043469 02/03/2005 In summary, Siemens is of the opinion that syngo®InSpace 4D Software Package does not introduce any n…
Siemens AG Medical Solutions2005—

Also cleared against K043469: 4 other devices →

What descends from it? (172)

See all 172

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

NumberDeviceApplicantDecidedDescendants
K073003Syngo Dual Energy with Extended FunctionallySiemens Medi Cal Solutions, Inc.2008168
K111079Syngo.Via Web ViewerSiemens AG Medical Solutions20111
K120331Syngo CT Dynamic AngioSiemens AG Medical Solutions20120

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

No FDA recall names this device.

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.

  • K250443MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.MobileSiemens Healthcare GmbH · 2025 · 7 generations on · ◆ in the 2025 descendants bar of FIG. 12 Class I recalls

What does this lineage say?

  • The line of descent spans 11 years and passes through 5 companies; a new generation was cleared every 2.4 years on median.
  • 1 of the 8 ancestors has a recall of any class.
  • Of its descendants, K073003 (Siemens Medi Cal Solutions, Inc., 2008) has gone furthest, with 168 descendants of its own.
  • 4 other devices also cite its predicate K043469.

How does its category compare?

All JAK devices

JAK System, X-Ray, Tomography, Computed: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JAK

27in 2025

2007: 142008: 262009: 152010: 72011: 162012: 282013: 172014: 302015: 302016: 252017: 292018: 242019: 282020: 302021: 202022: 302023: 272024: 262025: 272026 (partial year): 21
2007high 30 (2014) · low 7 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JAK

141in 2025

2007: 27 days median2008: 42 days median2009: 31 days median2010: 92 days median2011: 155 days median2012: 121 days median2013: 132 days median2014: 200 days median2015: 140 days median2016: 129 days median2017: 96 days median2018: 114 days median2019: 94 days median2020: 112 days median2021: 145 days median2022: 131 days median2023: 139 days median2024: 141 days median2025: 141 days median2026 (partial year): 167 days median
2007high 200 (2014) · low 27 (2007)2026

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

Recalls per year · JAK

17in 2025

2007: 112008: 162009: 292010: 512011: 342012: 232013: 112014: 102015: 282016: 442017: 332018: 102019: 52020: 82021: 152022: 92023: 92024: 202025: 172026 (partial year): 23
2007high 51 (2010) · low 5 (2019)2026

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

Adverse event reports per year · JAK

219in 2025

2007: 762008: 1202009: 1052010: 1192011: 2052012: 1922013: 4142014: 3082015: 4542016: 3652017: 3382018: 5432019: 2332020: 1772021: 2612022: 1992023: 3102024: 2122025: 219
2007high 543 (2018) · low 76 (2007)2025

MAUDE reports naming product code JAK, 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
200714271176
2008264216120
2009153129105
201079251119
20111615534205
20122812123192
20131713211414
20143020010308
20153014028454
20162512944365
2017299633338
20182411410543
201928945233
2020301128177
20212014515261
2022301319199
2023271399310
20242614120212
20252714117219
20262116723—

What is it indicated for?

syngo® InSpace 4D - Software Package is a self-contained image analysis software package. This real-time interactive evaluation in space and time for CT volume data sets provides the reconstruction of two-dimensional images into a three-dimensional image format. InSpace can be used to assist the physician in the diagnosis of blood vessels on the basis of a CT Angiography dataset (CTA). For a CTA examination a contrast media (CM) is administered into the…

Read the full statement (238 words)

syngo® InSpace 4D - Software Package is a self-contained image analysis software package. This real-time interactive evaluation in space and time for CT volume data sets provides the reconstruction of two-dimensional images into a three-dimensional image format.

InSpace can be used to assist the physician in the diagnosis of blood vessels on the basis of a CT Angiography dataset (CTA). For a CTA examination a contrast media (CM) is administered into the patient's blood vessels to enhance the contrast of the vessels in the CTA dataset, i.e. high values for the Hounsfield Unit (HU).

The goal is to visualize the blood vessels without other interfering anatomical structures.

The syngo® InSpace 4D is developed to facilitate a precise diagnosis by removing bone structures from a CTA data set. It can be used in the same way for Non CTA datasets to remove bones or extract and display selected bones, e.g. for the analysis of a fracture.

Additionally syngo® InSpace 4D is developed to facilitate fast and precise diagnosis by removing the CT table from a CT data set.

Furthermore the syngo® InSpace 4D is embedded in the framework of a new server/client architecture also referred to as syngo® WebSpace. The. server supports muitiple sessions from remote “thin client” terminals at the same time. The thin client application is also a part of the syngo® WebSpace software suite, installed on a different computer, connected to the server by a network.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K062673: Modification to Syngo Inspace 4D.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K062673

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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