510(k) Report

510(k) · Cleared

Cleared

SoloAsisst II, Voice Control

K200473510(k) TraditionalCleared Dec 22, 2020300-day reviewClass II21 CFR 876.1500

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

Aktormed GmbH · NAY System, Surgical, Computer Controlled Instrument

Cleared on Dec 22, 2020 as substantially equivalent to K171947 (Aktormed GmbH, 2018) after a 300-day review. Its family tree reaches back 5 generations to 1993. 2 later devices descend from it.

Decided
Dec 22, 2020
Review
300 days
Class
Class II
Product code
NAY
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K931783 (1993). 2 later devices descend from it, 1 citing it directly.

  1. Root · 5 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
  2. 4 generations backK960655 Aesop System and AccessoriesComputer Motion, Inc. · 1996
  3. 3 generations backK963126 Aesop System and AccessoriesComputer Motion, Inc. · 1997
  4. 2 generations backK972699 Aesop 3000 System and AccessoriesComputer Motion, Inc. · 1997
  5. 1 generation backK171947 Soloassist IIAktormed GmbH · 2018
  6. This deviceK200473 SoloAsisst II, Voice ControlAktormed GmbH · 2020
  7. Descendant · cites it directly · 1 of its ownK233312 SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426)…Aktormed GmbH · 2024
  8. Descendant · 2 generations on · 0 of its ownK261573 Endoscope Holder (182214)Aktormed GmbH · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K233312SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426) + ARTip solo voice…Aktormed GmbH · 2024 · cites it directly1descendant
  • K261573Endoscope Holder (182214)Aktormed GmbH · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K931783Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc.1993—
−4K960655Aesop System and AccessoriesComputer Motion, Inc.1996—
−3K963126Aesop System and AccessoriesComputer Motion, Inc.1997—
−2K972699Aesop 3000 System and AccessoriesComputer Motion, Inc.1997—
−1K171947Soloassist IIAktormed GmbH2018—
0 (this device)K200473SoloAsisst II, Voice ControlAktormed GmbH2020—
+1K233312SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426) + ARTip…Aktormed GmbH2024—
+2K261573Endoscope Holder (182214)Aktormed GmbH2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202610
FIG. 1 — Lineage of K200473, 1993–2026Source: 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.

Planning a device in NAY? 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 NAY device

  1. #1 K232610 da Vinci Surgical System Model IS5000, da…score 32.9 · 24 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
*K171947Soloassist II
Summary page 5
…Class II (i.e., whether it is unclassified or a class I, II, or III device) Predicate Device 510(k) Number K171947 Reference Device Manufacturer / 510(k)Submitter COMPUTER MOTION, INC. (Company Name) D…
Aktormed GmbH2018—
†K972699Aesop 3000 System and AccessoriesComputer Motion, Inc.1997—

Also cleared against K171947: 1 other device →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K233312SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426) + ARTip solo voice…Aktormed GmbH20241

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 27 years and passes through 2 companies; a new generation was cleared every 2.3 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K233312 (Aktormed GmbH, 2024) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K171947.

How does its category compare?

All NAY devices

NAY System, Surgical, Computer Controlled Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NAY

16in 2025

2008: 42009: 32010: 12011: 72012: 42013: 42014: 92015: 32016: 82017: 162018: 152019: 82020: 92021: 112022: 62023: 52024: 102025: 162026 (partial year): 7
2007high 16 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NAY

117in 2025

2008: 189 days median2009: 253 days median2011: 191 days median2012: 106 days median2013: 144 days median2014: 143 days median2015: 99 days median2016: 197 days median2017: 107 days median2018: 152 days median2019: 73 days median2020: 212 days median2021: 61 days median2022: 57 days median2023: 141 days median2024: 126 days median2025: 117 days median2026 (partial year): 89 days median
2007high 253 (2009) · low 57 (2022)2026

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

Recalls per year · NAY

1in 2025

2007: 112008: 32009: 12011: 22012: 12013: 62014: 252015: 32016: 12017: 12018: 22019: 52021: 32022: 32023: 2, 1 Class I2024: 402025: 12026 (partial year): 4, 1 Class I
2007high 40 (2024) · low 0 (2010)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · NAY

48,456in 2025

2007: 1332008: 2242009: 3802010: 6232011: 5012012: 1,5522013: 6,2172014: 6,1352015: 1,7222016: 1,0772017: 1,0492018: 1,0742019: 1,1542020: 1,5582021: 1,9972022: 5,7272023: 10,8982024: 12,8722025: 48,456
2007high 48,456 (2025) · low 133 (2007)2025

MAUDE reports naming product code NAY, 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
20070—11133
200841893224
200932531380
20101—0623
201171912501
2012410611,552
2013414466,217
20149143256,135
201539931,722
2016819711,077
20171610711,049
20181515221,074
201987351,154
2020921201,558
2021116131,997
202265735,727
202351412 (1)10,898
2024101264012,872
202516117148,456
20267894 (1)—

What is it indicated for?

The intended use of the SOLOASSIST II is a robotic computer driven system whose function is to hold and position a rigid laparoscope / endoscope. The SOLOASSIST II is indicated for use in minimally invasive interventions where a rigid laparoscope / endoscope is indicated for use. Surgeries, SOLOASSIST II is used, are laparoscopic cholecystectomy, laparoscopic hernia repair, laparoscopic appendectomy, laparoscopic pelvic lymph node dissection…

Read the full statement (126 words)

The intended use of the SOLOASSIST II is a robotic computer driven system whose function is to hold and position a rigid laparoscope / endoscope.

The SOLOASSIST II is indicated for use in minimally invasive interventions where a rigid laparoscope / endoscope is indicated for use. Surgeries, SOLOASSIST II is used, are laparoscopic cholecystectomy, laparoscopic hernia repair, laparoscopic appendectomy, laparoscopic pelvic lymph node dissection, laparoscopically assisted hysterectomy, laparoscopic & thorascopic, decompression fixation, wedge resection, lung biopsy, pleural biopsy, dorsal sympathectomy, pleurodesis, internal mammary artery dissection for coronary artery bypass, coronary artery bypass grafting where endoscopic visualization is indicated and examination of the evacuated cardiac chamber during performance of valve replacement.

The users of the SOLOASSIST II are general surgeons, gynecologists, cardiac surgeon, thoracic surgeon and urologists.

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. “K200473: SoloAsisst II, Voice Control.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K200473

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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