Skater Biliary Catheter
FDA 510(k) K070610 · Angiotech
510(k) numberK070610
Submission
- Device name
- Skater Biliary Catheter
- Applicant
- Angiotech
Herndon, VA, US - Received
- March 5, 2007
- Decision date
- June 21, 2007
- Decision
- Substantially Equivalent (SESE)
- 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
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| 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 |
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| K120827 | Quill Pdo Knotless Tissue-Closure Device (Polydixanone)NEW · Traditional | 07/13/2012SE |
| K113744 | Quill Pdo Knotless Tissue-Closure Device (Polydioxanone)NEW · Traditional | 02/01/2012SE |
| K113800 | Quill Quadrahelix Tissue-Closure DeviceGAW · Special | 01/20/2012SE |
| K073672 | Skater Biliary CatheterFGE · Special | 01/24/2008SE |
Questions and answers
When was Skater Biliary Catheter cleared by the FDA?
Skater Biliary Catheter (K070610) received a 510(k) decision of Substantially Equivalent on June 21, 2007, 108 days after the submission was received.
What is the product code of K070610?
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.