The following data is part of a premarket notification filed by Biomet Microfixation, Inc. with the FDA for Fracture/reconstruction System (traumaone).
| Device ID | K081067 |
| 510k Number | K081067 |
| Device Name: | FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE) |
| Classification | Plate, Bone |
| Applicant | BIOMET MICROFIXATION, INC. 1520 TRADEPORT DR. Jacksonville, FL 32218 |
| Contact | Kim Reed |
| Correspondent | Kim Reed BIOMET MICROFIXATION, INC. 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 | 2008-04-15 |
| Decision Date | 2008-05-09 |
| Summary: | summary |