FDA 510(k) Applications Submitted by BIOMET MICROFIXATION, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K091058 04/13/2009 ADKINS STRUT BIOMET MICROFIXATION, INC.
K081067 04/15/2008 FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE) BIOMET MICROFIXATION, INC.
K071577 06/08/2007 BIOMET MICROFIXATION LACTOSORB PECTUS STABILIZER BIOMET MICROFIXATION, INC.
K111908 07/05/2011 BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM BIOMET MICROFIXATION, INC.
K110574 03/01/2011 BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM BIOMET MICROFIXATION, INC.


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