K113651 is an FDA 510(k) clearance for the INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM. This device is classified as a Device, Vascular, For Promoting Embolization (Class II - Special Controls, product code KRD).
Submitted by Boston Scientific Corporation (Maple Grove, US). The FDA issued a Cleared decision on January 11, 2012, 30 days after receiving the submission on December 12, 2011.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.3300.
| 510(k) Number | K113651 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 12, 2011 |
| Decision Date | January 11, 2012 |
| Days to Decision | 30 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | KRD — Device, Vascular, For Promoting Embolization |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.3300 |