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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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