Synthes, Inc.
8 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY (K131792) | Synthes, Inc. | 2013-12-16 |
| SYNTHES PATIENT SPECIFIC PLATE (K122647) | Synthes, Inc. | 2013-02-28 |
| SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM (K113567) | Synthes, Inc. | 2012-11-19 |
| SYNTHES CURVILINEAR DISTRACTION SYSTEM (K121502) | Synthes, Inc. | 2012-08-23 |
| SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM (K121574) | Synthes, Inc. | 2012-06-29 |
| SYNTHES MATRIXMANDIBLE PERFORMED RECONSTRUCTION PLATES (K113251) | Synthes, Inc. | 2011-12-21 |
| SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS (K111323) | Synthes, Inc. | 2011-11-16 |
| SYNTHES STERNAL FIXATION SYSTEM (K112689) | Synthes, Inc. | 2011-10-26 |
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Every clearance here is in the API, with alerts when new ones post.