Biomet Microfixation, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Biomet Microfixation, Inc. has 5 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 5 cleared submissions from 2007 to 2011. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biomet Microfixation, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Nov 29, 2011
BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM
Orthopedic
147d
Cleared
May 18, 2011
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
Orthopedic
78d
Cleared
Jul 22, 2009
ADKINS STRUT
Orthopedic
100d
Cleared
May 09, 2008
FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE)
Dental
24d
Cleared
Sep 06, 2007
BIOMET MICROFIXATION LACTOSORB PECTUS STABILIZER
Orthopedic
90d