510(k) Report

510(k) · Decided

Decided

Bridge SE Self-Expanding Stent Delivery System

K011080510(k) TraditionalDecided Oct 11, 2001185-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

Medtronic Ave, Inc. · FGE Stents, Drains And Dilators For The Biliary Ducts

Cleared on Oct 11, 2001 after a 185-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 28 later devices descend from it.

Decided
Oct 11, 2001
Review
185 days
Class
Class II
Product code
FGE
Recalls
None
Predicates
0

28 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2002: 4 descendants cleared2003: 8 descendants cleared2004: 2 descendants cleared2005: 1 descendant cleared2006: 2 descendants cleared2008: 4 descendants cleared2013: 2 descendants cleared2010: 2 descendants cleared2012: 2 descendants cleared2011: 1 descendant cleared200020052010201520202025
  1. This deviceK011080 Bridge SE Self-Expanding Stent Delivery SystemMedtronic Ave, Inc. · 2001
  2. Descendant · cites it directly · 24 of its ownK021898 Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp. · 2002 · Recalled
  3. Descendant · 2 generations on · 10 of its ownK031777 Modeification to: Smart Control Nitinol Stent Transhepatic Biliary…Cordis Corp. · 2003 · Recalled
  4. Descendant · 2 generations on · 9 of its ownK032457 Modification to Smart Control Nitinol Stent Transhepatic Biliary…Cordis Corp. · 2003
  5. Descendant · 3 generations on · 6 of its ownK060557 Suresave TM Self-Expandable Nitinol Stent and Precision TM Delivery…Idev Technologies, Inc. · 2006
  6. Descendant · 4 generations on · 5 of its ownK071646 Supera Interwoven Self-Expanding Biliary Nitinol Stent Delivery…Idev Technologies, Inc. · 2008

Showing 5 of 28 descendants. See all descendants

Descendants cleared per year

2002: 42003: 82004: 22005: 12006: 22008: 42010: 22011: 12012: 22013: 2
2002high 8 (2003) · low 0 (2007)2026

Most influential descendants

Showing 5 of 28 · See all
  • K021898Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp. · 2002 · cites it directly24descendants
  • K031777Modeification to: Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp. · 2003 · 2 generations on10descendants
  • K032457Modification to Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp. · 2003 · 2 generations on9descendants
  • K060557Suresave TM Self-Expandable Nitinol Stent and Precision TM Delivery Catheter-SS06120060Idev Technologies, Inc. · 2006 · 3 generations on6descendants
  • K071646Supera Interwoven Self-Expanding Biliary Nitinol Stent Delivery Catheter, Model #…Idev Technologies, Inc. · 2008 · 4 generations on5descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K011080Bridge SE Self-Expanding Stent Delivery SystemMedtronic Ave, Inc.2001—
+1K021898Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp.20021
+2K031777Modeification to: Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp.20033
+2K032457Modification to Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp.2003—
+3K060557Suresave TM Self-Expandable Nitinol Stent and Precision TM Delivery…Idev Technologies, Inc.2006—
+4K071646Supera Interwoven Self-Expanding Biliary Nitinol Stent Delivery Catheter…Idev Technologies, Inc.2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200240
200380
200420
200510
200620
200840
201020
201110
201220
201320
FIG. 1 — Lineage of K011080, 2001–2013Source: 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), 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (28)

See all 28

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

NumberDeviceApplicantDecidedDescendants
K021898Smart Control Nitinol Stent Transhepatic Biliary SystemCordis Corp.200224
K014205Modification to Bridge Self-Expanding Biliary Stent Delivery System (Bridge SE)Medtronic Ave, Inc.20022
K022026Medtronic Ave Bridge Polaris Biliary Stent System (Polaris)Medtronic Ave, Inc.20021

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?

  • Of its descendants, K021898 (Cordis Corp., 2002) has gone furthest, with 24 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.

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—

More from Medtronic Ave, Inc.

13 FDA decisions under this applicant name. See the company

  • K032768Medtronic, Inc. Racer Biliary Stent System (Racer), Model XD#YF (L)Medtronic Ave, Inc. · 20031 recall
  • K030633Medtronic Ave Bridge Constant Biliary Stent System or ('ConstantMedtronic Ave, Inc. · 2003
  • K030839Medtronic Ave Bridge Aurora Biliary Stent System (Aurora)Medtronic Ave, Inc. · 2003
  • K022026Medtronic Ave Bridge Polaris Biliary Stent System (Polaris)Medtronic Ave, Inc. · 2002
  • K014205Modification to Bridge Self-Expanding Biliary Stent Delivery System (Bridge SE)Medtronic Ave, Inc. · 2002

Recent decisions in FGE

The FGE category page

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  • K253393Single-use Balloon Dilatation Catheter (AG-5251-083018 AG-5251-085518 AG-5251-088018 AG-5251-083019…Hangzhou AGS MedTech Co., Ltd. · 2026
  • K253832Dilation Balloon CatheterMirco-Tech (Nanjing) Co., Ltd. · 2026

https://510kreport.com/device/K011080 · printed Nov 4, 2026

Cite this page

510(k) Report. “K011080: Bridge SE Self-Expanding Stent Delivery System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K011080

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026