K150201 is an FDA 510(k) clearance for the Quick-Cross Extreme Support Catheter, Quick-Cross Select Support Catheter. This device is classified as a Catheter, Percutaneous (Class II - Special Controls, product code DQY).
Submitted by Spectranetics, Inc. (Colorado Springs, US). The FDA issued a Cleared decision on February 27, 2015, 29 days after receiving the submission on January 29, 2015.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1250.
| 510(k) Number | K150201 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 29, 2015 |
| Decision Date | February 27, 2015 |
| Days to Decision | 29 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Statement |
| Product Code | DQY - Catheter, Percutaneous |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1250 |