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 |