The following data is part of a premarket notification filed by Biomet Trauma with the FDA for Lower Extremity External Fixation - Expanded Indications.
Device ID | K081244 |
510k Number | K081244 |
Device Name: | LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | BIOMET TRAUMA P.O. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Patricia S Beres |
Correspondent | Patricia S Beres BIOMET TRAUMA P.O. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-05-01 |
Decision Date | 2008-07-30 |
Summary: | summary |