Biomet Trauma

FDA Filings

This page includes the latest FDA filings for Biomet Trauma. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMN K091976 BIOMET TRAUMA	BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAIL	2009-08-17
PMN K092078 BIOMET TRAUMA	OPTILOCK PERIARTICULAR PLATING	2009-08-05
PMN K082874 BIOMET TRAUMA	BIODRIVE CANNULATED SCREW SYSTEM	2009-02-05
PMN K081244 BIOMET TRAUMA	LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS	2008-07-30
PMN K081243 BIOMET TRAUMA	BIOMET PHOENIX ANKLE NAIL SYSTEM	2008-06-27
PMN K071325 BIOMET TRAUMA	BIOMET VARIABLE LOCKING PLATE SYSTEM	2007-07-26
PMN K070823 BIOMET TRAUMA	GROWTH CONTROL PLATING SYSTEM	2007-05-07

Similar & Related FDA Registered Companies

• BIOMET TRAUMA (AKA EBI LLC)
• BIOMET TRAUMA (AKA EBI, LP)