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 |