510(k) · Cleared
ClearedIntracoil Peripheral Stent
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Intratherapeutics, Inc. · JCT Prosthesis, Tracheal, Expandable
Cleared on Jun 2, 1999 as substantially equivalent to K963241 (Boston Scientific Corp, 1996) and 1 other predicate after a 131-day review. Its family tree reaches back 6 generations to 1992. 1 later device descends from it.
- Decided
- Jun 2, 1999
- Review
- 131 days
- Class
- Class II
- Product code
- JCT
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 6 generations to K923119 (1992). 16 ancestors in all, the oldest K911292 (1991). 1 later device descends from it, 1 citing it directly.
- Root · 6 generations backK923119 Wallstent Esophageal ProthesisSchneider U.S. Stent Div. · 1992
- 5 generations backK945494 Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1995 · Recalled
- 4 generations backK961296 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
- 3 generations backK964121 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
- 2 generations backK980163 Wallstent Tracheobronchial Endoprosthesis and Wallstent…Boston Scientific Scimed, Inc. · 1998 · Recalled
- 1 generation backK982184 Wallstent EndoprosthesisBoston Scientific Scimed, Inc. · 1998
- This deviceK990221 Intracoil Peripheral StentIntratherapeutics, Inc. · 1999
- Descendant · cites it directly · 0 of its ownK021563 Intracoil Self-Expanding Peripheral StentSulzer Intratherapeutics, Inc. · 2002
Most influential descendants
Showing 1 of 1 · See all- K021563Intracoil Self-Expanding Peripheral StentSulzer Intratherapeutics, Inc. · 2002 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K923119 | Wallstent Esophageal Prothesis | Schneider U.S. Stent Div. | 1992 | — |
| −5 | K945494 | Wallstent (R) Tracheobronchial Endoprosthesis | Boston Scientific Scimed, Inc. | 1995 | 1 |
| −4 | K961296 | Wallstent Tracheobronchial Endoprosthesis | Boston Scientific Scimed, Inc. | 1996 | 1 |
| −3 | K964121 | Wallstent Tracheobronchial Endoprosthesis | Boston Scientific Scimed, Inc. | 1996 | 1 |
| −2 | K980163 | Wallstent Tracheobronchial Endoprosthesis and Wallstent Tracheobronchial… | Boston Scientific Scimed, Inc. | 1998 | 1 |
| −1 | K982184 | Wallstent Endoprosthesis | Boston Scientific Scimed, Inc. | 1998 | — |
| 0 (this device) | K990221 | Intracoil Peripheral Stent | Intratherapeutics, Inc. | 1999 | — |
| +1 | K021563 | Intracoil Self-Expanding Peripheral Stent | Sulzer Intratherapeutics, Inc. | 2002 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1991 | 2 | 0 |
| 1994 | 3 | 0 |
| 1996 | 3 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 1 | 0 |
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 JCT? 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 JCT device
- #1 K230269 Ultraflex™ Tracheobronchial Stent Systemscore 8.1 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K963241 | UltraflexSummary page 4…s premarket notification submission. Substantial equivalence is claimed to the Boston Scientific, Inc. Ultraflex™ and Wallstent® self- expanding tracheobronchial stents (K963241 and K982184, respectively). The IntraCoil® Stent is a self-expanding nickel-titanium (Nitinol) coil premounted on a delivery cat… | 1996 |
| * | K982184 | Wallstent EndoprosthesisSummary page 4…notification submission. Substantial equivalence is claimed to the Boston Scientific, Inc. Ultraflex™ and Wallstent® self- expanding tracheobronchial stents (K963241 and K982184, respectively). The IntraCoil® Stent is a self-expanding nickel-titanium (Nitinol) coil premounted on a delivery catheter. The s… | 1998 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K021563 | Intracoil Self-Expanding Peripheral Stent | 2002 | 0 |
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 7 years and passes through 3 companies; a new generation was cleared every 1.3 years on median.
- 5 of the 16 ancestors have a recall of any class.
- Of its descendants, K021563 (Sulzer Intratherapeutics, Inc., 2002) has gone furthest, with 0 descendants of its own.
- 8 other devices also cite its predicate K963241.
How does its category compare?
All JCT devicesJCT Prosthesis, Tracheal, Expandable: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JCT
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · JCT
234in 2014
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JCT
2in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JCT
50in 2025
MAUDE reports naming product code JCT, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 2 | — | 0 | 150 |
| 2008 | 1 | — | 0 | 143 |
| 2009 | 1 | — | 0 | 163 |
| 2010 | 0 | — | 46 | 147 |
| 2011 | 0 | — | 2 | 95 |
| 2012 | 1 | — | 0 | 109 |
| 2013 | 0 | — | 0 | 238 |
| 2014 | 3 | 234 | 0 | 168 |
| 2015 | 0 | — | 0 | 251 |
| 2016 | 1 | — | 0 | 217 |
| 2017 | 0 | — | 0 | 109 |
| 2018 | 1 | — | 0 | 122 |
| 2019 | 0 | — | 0 | 106 |
| 2020 | 1 | — | 0 | 120 |
| 2021 | 2 | — | 0 | 106 |
| 2022 | 1 | — | 0 | 61 |
| 2023 | 1 | — | 0 | 110 |
| 2024 | 0 | — | 0 | 74 |
| 2025 | 0 | — | 0 | 50 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The IntraCoil® Peripheral Stent is indicated for use in the treatment of bronchial strictures produced by malignant neoplasms.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K990221 · printed Nov 6, 2026
Cite this page
510(k) Report. “K990221: Intracoil Peripheral Stent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K990221
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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