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 |