The following data is part of a premarket notification filed by Biomet Trauma with the FDA for Biodrive Cannulated Screw System.
| Device ID | K082874 |
| 510k Number | K082874 |
| Device Name: | BIODRIVE CANNULATED SCREW SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | BIOMET TRAUMA 100 INTERPACE PARKWAY Parsippany, NJ 07054 |
| Contact | Debra L Bing |
| Correspondent | Debra L Bing BIOMET TRAUMA 100 INTERPACE PARKWAY Parsippany, NJ 07054 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-29 |
| Decision Date | 2009-02-05 |
| Summary: | summary |