The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Biomet Headless Compression And Twist-off Screws.
| Device ID | K142658 |
| 510k Number | K142658 |
| Device Name: | Biomet Headless Compression And Twist-off Screws |
| Classification | Screw, Fixation, Bone |
| Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46582 |
| Contact | Victoria Scheitlin |
| Correspondent | Victoria Scheitlin BIOMET MANUFACTURING CORP. 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 | 2014-09-18 |
| Decision Date | 2014-11-13 |
| Summary: | summary |