Biomet Microfixation · Class II · Cleared Jun 29, 2012
| K-number | K113512 |
| Device name | BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES AND PREBENT PLATES SYSTEM |
| Applicant | Biomet Microfixation |
| Product code | JEY |
| Device class | Class II |
| Decision date | Jun 29, 2012 |
| 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