Corentec Co., Ltd. · Class II · Cleared Dec 5, 2016
| K-number | K162127 |
| Device name | Bencox M Stem Lateralized & Bencox Mirabo Cup System |
| Applicant | Corentec Co., Ltd. |
| Product code | LPH |
| Device class | Class II |
| Decision date | Dec 5, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 888.3358 |
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