The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Thp Hip Fracture Plating System.
Device ID | K173826 |
510k Number | K173826 |
Device Name: | THP Hip Fracture Plating System |
Classification | Device, Fixation, Proximal Femoral, Implant |
Applicant | Biomet, Inc. 56 East Bell Drive Warsaw, IN 46582 |
Contact | Annette Minthorn |
Correspondent | Annette Minthorn Biomet, Inc. 56 East Bell Drive Warsaw, IN 46582 |
Product Code | JDO |
Subsequent Product Code | HWC |
Subsequent Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-18 |
Decision Date | 2018-02-07 |
Summary: | summary |