K170059 is an FDA 510(k) clearance for the Spectranetics Turbo-Elite Laser Atherectomy Catheters. This device is classified as a Catheter, Peripheral, Atherectomy (Class II - Special Controls, product code MCW).
Submitted by Spectranetics, Inc. (Colorado Springs, US). The FDA issued a Cleared decision on April 7, 2017, 91 days after receiving the submission on January 6, 2017.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4875.
| 510(k) Number | K170059 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 06, 2017 |
| Decision Date | April 07, 2017 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | MCW — Catheter, Peripheral, Atherectomy |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4875 |