| K-number | K862139 |
| Device name | IMTECH FIXATION SYSTEMS |
| Applicant | Imtech, Inc. |
| Product code | JEY |
| Device class | Class II |
| Decision date | Jul 16, 1986 |
| Decision | Substantially Equivalent |
| Regulation | 872.4760 |
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