K171487 is an FDA 510(k) clearance for the Sirius MRI Marker NS. This device is classified as a Source, Brachytherapy, Radionuclide (Class II - Special Controls, product code KXK).
Submitted by C4 Imaging, LLC (Doylestown, US). The FDA issued a Cleared decision on August 25, 2017, 95 days after receiving the submission on May 22, 2017.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.5730.
| 510(k) Number | K171487 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 22, 2017 |
| Decision Date | August 25, 2017 |
| Days to Decision | 95 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | KXK - Source, Brachytherapy, Radionuclide |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.5730 |