Genoss Co., Ltd. · Class II · Cleared Nov 19, 2010
| K-number | K102015 |
| Device name | OSTEON, OSTEON SINUS, OSTEON LIFTING |
| Applicant | Genoss Co., Ltd. |
| Product code | LYC |
| Device class | Class II |
| Decision date | Nov 19, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 872.3930 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov