The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for 3.omm Biomet Cannulated Screw System.
Device ID | K143188 |
510k Number | K143188 |
Device Name: | 3.Omm Biomet Cannulated Screw System |
Classification | Screw, Fixation, Bone |
Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46581 |
Contact | Victoria Scheitlin |
Correspondent | Suzana Otaño BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46581 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-11-05 |
Decision Date | 2014-12-30 |
Summary: | summary |