K150692 is an FDA 510(k) clearance for the AXIOS Stent with Electrocautery Enhanced Delivery System. This device is classified as a Pancreatic Stent, Covered, Metallic, Removable (Class II - Special Controls, product code PCU).
Submitted by Boston Scientific Corp (Mountain View, US). The FDA issued a Cleared decision on August 5, 2015, 140 days after receiving the submission on March 18, 2015.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5015. To Facilitate Transmural Endoscopic Drainage Of Pancreatic Pseudocysts.
| 510(k) Number | K150692 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 18, 2015 |
| Decision Date | August 05, 2015 |
| Days to Decision | 140 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | PCU — Pancreatic Stent, Covered, Metallic, Removable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.5015 |
| Definition | To Facilitate Transmural Endoscopic Drainage Of Pancreatic Pseudocysts |