Duramax .018 Biliary Stent System
FDA 510(k) K032436 · Avantec Vascular Corp.
510(k) numberK032436
Submission
- Device name
- Duramax .018 Biliary Stent System
- Applicant
- Avantec Vascular Corp.
Sunnyvale, CA, US - Received
- August 7, 2003
- Decision date
- February 4, 2004
- Decision
- Unknown (SESU)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FGE – Stents, Drains And Dilators For The Biliary Ducts
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5010
- Specialty
- Gastroenterology, Urology
- Implant
- Yes
- Life-sustaining
- Yes
Other 510(k)s with product code FGE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260835 | ARCHIMEDES Biodegradable Stent (Medium)FGE · Traditional | Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.) | 07/27/2026SE |
| K253393 | Single-use Balloon Dilatation Catheter (AG-5251-083018 AG-5251-085518 AG-5251-088018…FGE · Traditional | Hangzhou AGS MedTech Co., Ltd. | 06/24/2026SE |
| K253832 | Dilation Balloon CatheterFGE · Traditional | Mirco-Tech (Nanjing) Co., Ltd. | 04/24/2026SE |
| K251658 | Endoflux Biliary & Pancreatic Stent SetsFGE · Traditional | Medi-Globe GmbH | 04/16/2026SE |
| K253987 | BARE Wireguided Balloon Dilation Catheter (1235)FGE · Traditional | GIE Medical | 03/13/2026SE |
| K253132 | Single use stone retrieval balloonsFGE · Traditional | Zhejiang Chuangxiang Medical Technology Co., Ltd. | 03/06/2026SE |
| K251123 | Niti-S Biliary Stent; Niti-S Biliary Slim M StentFGE · Traditional | Taewoong Medical Co., Ltd. | 12/29/2025SESU |
| K251019 | BIOTEQ Drainage Catheter Set: BT-PD1-SERIES-G and BT-PDS-SERIES-GFGE · Traditional | Bioteque Corporation | 12/22/2025SE |
| K250409 | Disposable Balloon Catheter (B5-2Q); Disposable Balloon Catheter (B7-2Q); Disposable…FGE · Traditional | Olympus Medical Systems Corporation | 10/21/2025SE |
| K251229 | EndoFixTissue Fixation SystemFGE · Traditional | Softac Medical Technologies | 08/20/2025SE |
More from Softac Medical Technologies
| 510(k) | Device | Decision |
|---|---|---|
| K251207 | Sangria Thrombectomy SystemQEW · Traditional | 01/07/2026SE |
| K170987 | Captus Vascular Retrieval SystemMMX · Traditional | 08/28/2017SE |
| K030638 | Duramax .035 Biliary Stent System, Models DML0718-80, DML0718-135, DML0818-80…FGE · Traditional | 07/09/2003SESU |
| K030062 | Admiral .035 Dilatation Catheter, Models ADL0720-80,ADL0720-135,ADL0820-80…LIT · Traditional | 04/03/2003SE |
Questions and answers
When was Duramax .018 Biliary Stent System cleared by the FDA?
Duramax .018 Biliary Stent System (K032436) received a 510(k) decision of Unknown on February 4, 2004, 181 days after the submission was received.
What is the product code of K032436?
The FDA product code is FGE – Stents, Drains And Dilators For The Biliary Ducts, a Class II (moderate risk) device regulated under 21 CFR 876.5010.