The following data is part of a premarket notification filed by Biomet Inc with the FDA for Biomet Variable Pitch Compression Screw System.
Device ID | K160058 |
510k Number | K160058 |
Device Name: | Biomet Variable Pitch Compression Screw System |
Classification | Screw, Fixation, Bone |
Applicant | Biomet Inc 56 East Bell Drive Warsaw, IN 46582 |
Contact | Julie Largent |
Correspondent | Julie Largent Biomet Inc 56 East Bell Drive Warsaw, IN 46582 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-01-12 |
Decision Date | 2016-03-09 |
Summary: | summary |