K210125 is an FDA 510(k) clearance for the BonOs HV Genta, BonOs MV Genta, BonOs LV Genta. This device is classified as a Bone Cement (Class II - Special Controls, product code LOD).
Submitted by Osartis GmbH (Münster, DE). The FDA issued a Cleared decision on March 19, 2021, 59 days after receiving the submission on January 19, 2021.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3027.
| 510(k) Number | K210125 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 19, 2021 |
| Decision Date | March 19, 2021 |
| Days to Decision | 59 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | LOD - Bone Cement |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3027 |