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 |