| K-number | K890814 |
| Device name | DANEK RING FIXATOR (DRF) |
| Applicant | Danek Medical, Inc. |
| Product code | KTT |
| Device class | Class II |
| Decision date | Jun 13, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 888.3030 |
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