K113210 is an FDA 510(k) clearance for the ADVANTAGE-STRAND/ADVANTAGE-LOAD BRACHYTHERAPY KIT. This device is classified as a Source, Brachytherapy, Radionuclide (Class II - Special Controls, product code KXK).
Submitted by Isoaid, LLC (Port Richey, US). The FDA issued a Cleared decision on August 10, 2012, 283 days after receiving the submission on November 1, 2011.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.5730.
| 510(k) Number | K113210 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 01, 2011 |
| Decision Date | August 10, 2012 |
| Days to Decision | 283 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 |