The following data is part of a premarket notification filed by Biomet Microfixation with the FDA for Biomet Microfixation Mandibular Fracture/ Reconstruction Devices And Prebent Plates System.
| Device ID | K113512 |
| 510k Number | K113512 |
| Device Name: | BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES AND PREBENT PLATES SYSTEM |
| Classification | Plate, Bone |
| Applicant | BIOMET MICROFIXATION 1520 TRADEPORT DR. Jacksonville, FL 32218 |
| Contact | Sheryl Malmberg |
| Correspondent | Sheryl Malmberg BIOMET MICROFIXATION 1520 TRADEPORT DR. Jacksonville, FL 32218 |
| Product Code | JEY |
| CFR Regulation Number | 872.4760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-11-28 |
| Decision Date | 2012-06-29 |