The following data is part of a premarket notification filed by Biomet Manufacturing with the FDA for Biomet Proximal Humerus Plating System.
Device ID | K143697 |
510k Number | K143697 |
Device Name: | Biomet Proximal Humerus Plating System |
Classification | Plate, Fixation, Bone |
Applicant | Biomet Manufacturing 56 East Bell Drive, PO Box 587 Warsaw, IN 46582 |
Contact | Julie Largent |
Correspondent | Julie Largent Biomet Manufacturing 56 East Bell Drive, PO Box 587 Warsaw, IN 46582 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-12-24 |
Decision Date | 2015-03-30 |
Summary: | summary |