The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Tsp Hip Fracture Plating System.
Device ID | K140018 |
510k Number | K140018 |
Device Name: | TSP HIP FRACTURE PLATING SYSTEM |
Classification | Device, Fixation, Proximal Femoral, Implant |
Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Gary Baker |
Correspondent | Gary Baker BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | JDO |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-01-03 |
Decision Date | 2014-04-04 |
Summary: | summary |