Sonoma Orthopedic Products, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K161371 | Sonoma Fifth Metatarsal Repair System | HSB | 2017-02-24 | View |
| 510(k) | K111550 | SONOMA FASTRAC CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA FASTRAC XXYYY(X=DIA, YYY=LENGTH- IN MM) | HSB | 2011-08-19 | View |
| 510(k) | K100112 | SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA, YYY=LENGTH-IN MM) | HSB | 2010-09-28 | View |
| 510(k) | K092110 | WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX) | HSB | 2010-01-20 | View |
| 510(k) | K090304 | WAVEON WRX BONE FIXATION SYSTEM | HRS | 2009-08-28 | View |
| 510(k) | K081832 | ENSPLINTCMX CLAVICLE PIN | HSB | 2008-10-10 | View |
| 510(k) | K080778 | ENSPLINT TM BONE SCREW | HWC | 2008-07-10 | View |
| 510(k) | K071809 | ENSPLINTRX BONE FIXATION SYSTEM | HRS | 2008-02-21 | View |
No matching devices.
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