Biomet Microfixation, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111908 | BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM | HWC | 2011-11-29 | View |
| 510(k) | K110574 | BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM | HRS | 2011-05-18 | View |
| 510(k) | K091058 | ADKINS STRUT | HRS | 2009-07-22 | View |
| 510(k) | K081067 | FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE) | JEY | 2008-05-09 | View |
| 510(k) | K071577 | BIOMET MICROFIXATION LACTOSORB PECTUS STABILIZER | HRS | 2007-09-06 | View |
No matching devices.
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