Medyssey USA, Inc. · Class II · Cleared Jun 12, 2017
| K-number | K171509 |
| Device name | Iliad® Pedicle Screw System and Zenius® Pedicle Screw System |
| Applicant | Medyssey USA, Inc. |
| Product code | NKB |
| Device class | Class II |
| Decision date | Jun 12, 2017 |
| Decision | Substantially Equivalent |
| Regulation | 888.3070 |
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