510(k) Report

510(k) · Decided

Decided

Niti-S Biliary Stent

K073667510(k) AbbreviatedDecided Nov 19, 2008329-day reviewClass II21 CFR 876.5010

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

Taewoong Medical Co., Ltd. · FGE Stents, Drains And Dilators For The Biliary Ducts

Cleared on Nov 19, 2008 as substantially equivalent to K040930 (Wilson-Cook Medical, Inc., 2004) and 2 other predicates after a 329-day review. Its family tree reaches back 7 generations to 1992. 23 later devices descend from it.

Decided
Nov 19, 2008
Review
329 days
Class
Class II
Product code
FGE
Recalls
None
Predicates
3

Its longest line of descent runs back 7 generations to K923119 (1992). 23 ancestors in all, the oldest K911292 (1991). 23 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2004: 1 other ancestor2003: 1 other ancestor2002: 1 other ancestor2000: 1 other ancestor1997: 1 other ancestor1996: 3 other ancestors2001: 1 other ancestor1998: 1 other ancestor1994: 3 other ancestors1991: 2 other ancestors2010: 1 descendant cleared2022: 2 descendants cleared2012: 1 descendant cleared2025: 3 descendants cleared2023: 2 descendants cleared2011: 1 descendant cleared2014: 2 descendants cleared2021: 3 descendants cleared2019: 1 descendant cleared2013: 1 descendant cleared2020: 2 descendants cleared2018: 1 descendant cleared2024: 2 descendants cleared2026: 1 descendant clearedK923119 · Wallstent Esophageal Prothesis · Schneider U.S. Stent Div. · 1992K945494 · Wallstent (R) Tracheobronchial Endoprosthesis · Boston Scientific Scimed, Inc. · 1995 · recalledK961296 · Wallstent Tracheobronchial Endoprosthesis · Boston Scientific Scimed, Inc. · 1996 · recalledK964121 · Wallstent Tracheobronchial Endoprosthesis · Boston Scientific Scimed, Inc. · 1996 · recalled×2: 2 generations cleared close together, K980163 (1998), K982184 (1998) K012752 · Wallstent RX Biliary Endoprostheses, Models 6961-6972 Inclusive · Boston Scientific Corp · 2001 · recalled1990200020102020
  1. Root · 7 generations backK923119 Wallstent Esophageal ProthesisSchneider U.S. Stent Div. · 1992
  2. 6 generations backK945494 Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1995 · Recalled
  3. 5 generations backK961296 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
  4. 4 generations backK964121 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
  5. 3 generations backK980163 Wallstent Tracheobronchial Endoprosthesis and Wallstent…Boston Scientific Scimed, Inc. · 1998 · Recalled
  6. 2 generations backK982184 Wallstent EndoprosthesisBoston Scientific Scimed, Inc. · 1998
  7. 1 generation backK012752 Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp · 2001 · Recalled
  8. This deviceK073667 Niti-S Biliary StentTaewoong Medical Co., Ltd. · 2008
  9. Descendant · cites it directly · 10 of its ownK113551 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2012 · Recalled
  10. Descendant · 2 generations on · 9 of its ownK123205 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2013 · Recalled
  11. Descendant · cites it directly · 6 of its ownK111149 Hanarostent Biliary (NNN)M.I.Tech Co., Ltd. · 2011
  12. Descendant · 2 generations on · 3 of its ownK211706 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2021
  13. Descendant · 3 generations on · 3 of its ownK180144 Agile Esophageal Stent SystemBoston Scientific Corporation · 2018

Showing 5 of 23 descendants. See all descendants

Descendants cleared per year

2010: 12011: 12012: 12013: 12014: 22018: 12019: 12020: 22021: 32022: 22023: 22024: 22025: 32026: 1
2010high 3 (2021) · low 0 (2015)2026

Most influential descendants

Showing 5 of 23 · See all
  • K113551Esophageal TTS StentTaewoong Medical Co., Ltd. · 2012 · cites it directly10descendants
  • K123205Esophageal TTS StentTaewoong Medical Co., Ltd. · 2013 · 2 generations on9descendants
  • K111149Hanarostent Biliary (NNN)M.I.Tech Co., Ltd. · 2011 · cites it directly6descendants
  • K211706Esophageal TTS StentTaewoong Medical Co., Ltd. · 2021 · 2 generations on3descendants
  • K180144Agile Esophageal Stent SystemBoston Scientific Corporation · 2018 · 3 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K923119Wallstent Esophageal ProthesisSchneider U.S. Stent Div.1992—
−6K945494Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19951
−5K961296Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19961
−4K964121Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19961
−3K980163Wallstent Tracheobronchial Endoprosthesis and Wallstent Tracheobronchial…Boston Scientific Scimed, Inc.19981
−2K982184Wallstent EndoprosthesisBoston Scientific Scimed, Inc.1998—
−1K012752Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp20011
0 (this device)K073667Niti-S Biliary StentTaewoong Medical Co., Ltd.2008—
+1K113551Esophageal TTS StentTaewoong Medical Co., Ltd.20121
+2K123205Esophageal TTS StentTaewoong Medical Co., Ltd.20131
+1K111149Hanarostent Biliary (NNN)M.I.Tech Co., Ltd.2011—
+2K211706Esophageal TTS StentTaewoong Medical Co., Ltd.2021—
+3K180144Agile Esophageal Stent SystemBoston Scientific Corporation2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199120
199430
199630
199710
199810
200010
200110
200210
200310
200410
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201110
201210
201310
201420
201810
201910
202020
202130
202220
202320
202420
202530
202610
FIG. 1 — Lineage of K073667, 1992–2026Source: 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 FGE? 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 FGE device

  1. #1 K240464 WallFlex Biliary RX Stent System; Epic Biliary…score 14.5 · 13 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
*K040930Zilver Biliary Stent System Usw
Summary page 1
…Product Code: FGE Third Party Reviewed: NO 3. Predicate Device: 1) Zilver Biliary Stent System USW, K040930 2) Wallstent RX Biliary Endoprostheses, K012752 3) Niti-S Stent & Introducer, Model Esophageal, K041 648 4…
Wilson-Cook Medical, Inc.2004—
*K012752Wallstent RX Biliary Endoprostheses, Models 6961-6972 Inclusive
Summary page 1
…rd Party Reviewed: NO 3. Predicate Device: 1) Zilver Biliary Stent System USW, K040930 2) Wallstent RX Biliary Endoprostheses, K012752 3) Niti-S Stent & Introducer, Model Esophageal, K041 648 4. Description: The proposed Niti-S Biliar…
Boston Scientific Corp20011
*K041648Niti-S Stent & Introducer, Model Eoxxxx
Summary page 1
…1) Zilver Biliary Stent System USW, K040930 2) Wallstent RX Biliary Endoprostheses, K012752 3) Niti-S Stent & Introducer, Model Esophageal, K041 648 4. Description: The proposed Niti-S Biliary Stent consists of an implantable metallic stent and a flexible…
Taewoong Medical Co., Ltd.2005—

What descends from it? (23)

See all 23

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

NumberDeviceApplicantDecidedDescendants
K113551Esophageal TTS StentTaewoong Medical Co., Ltd.201210
K111149Hanarostent Biliary (NNN)M.I.Tech Co., Ltd.20116
K093003Bonastent BiliaryEndochoice, Inc.20103
K221071Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd.20221
K251123Niti-S Biliary Stent; Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd.20250
K223626Niti-S Biliary Speed D StentTaewoong Medical Co., Ltd.20230

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 16 years and passes through 4 companies; a new generation was cleared every 1.4 years on median.
  • 8 of the 23 ancestors have a recall of any class.
  • Of its descendants, K113551 (Taewoong Medical Co., Ltd., 2012) has gone furthest, with 10 descendants of its own.

How does its category compare?

All FGE devices

FGE Stents, Drains And Dilators For The Biliary Ducts: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · FGE

7in 2025

2007: 42008: 112009: 72010: 92011: 92012: 82013: 52014: 82015: 82016: 42017: 92018: 72019: 22020: 42021: 12022: 62023: 62024: 62025: 72026 (partial year): 8
2007high 11 (2008) · low 1 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FGE

257in 2025

2007: 316 days median2008: 214 days median2009: 160 days median2010: 81 days median2011: 114 days median2012: 96 days median2013: 161 days median2014: 156 days median2015: 79 days median2016: 49 days median2017: 59 days median2018: 215 days median2020: 121 days median2022: 101 days median2023: 199 days median2024: 188 days median2025: 257 days median2026 (partial year): 153 days median
2007high 316 (2007) · low 49 (2016)2026

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

Recalls per year · FGE

1in 2024

2007: 542008: 932009: 182010: 322011: 22012: 42013: 32017: 12018: 432019: 132020: 12021: 272022: 212023: 192024: 12026 (partial year): 11
2007high 93 (2008) · low 0 (2014)2026

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

Adverse event reports per year · FGE

1,923in 2025

2007: 1,0062008: 1,4652009: 1,6552010: 1,4342011: 1,3212012: 1,1832013: 1,0602014: 1,2702015: 1,5432016: 1,4532017: 1,5152018: 1,6812019: 1,8962020: 2,1822021: 2,2972022: 1,7492023: 1,6152024: 1,9482025: 1,923
2007high 2,297 (2021) · low 1,006 (2007)2025

MAUDE reports naming product code FGE, 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
20074316541,006
200811214931,465
20097160181,655
2010981321,434
2011911421,321
201289641,183
2013516131,060
2014815601,270
201587901,543
201644901,453
201795911,515
20187215431,681
20192—131,896
2020412112,182
20211—272,297
20226101211,749
20236199191,615
2024618811,948
2025725701,923
2026815311—

What is it indicated for?

Niti-S Biliary Stent is indicated for the palliation of malignant strictures in the biliary tree.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K073667: Niti-S Biliary Stent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K073667

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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