The following data is part of a premarket notification filed by Biomet Inc. with the FDA for A. L. P. S. Clavicle Plating System.
Device ID | K173767 |
510k Number | K173767 |
Device Name: | A. L. P. S. Clavicle Plating System |
Classification | Plate, Fixation, Bone |
Applicant | Biomet Inc. 56 East Bell Drive Warsaw, IN 46582 |
Contact | Dhaval Saraiya |
Correspondent | Dhaval Saraiya Biomet Inc. 56 East Bell Drive 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 | 2017-12-11 |
Decision Date | 2018-04-06 |
Summary: | summary |