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Synthes, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K131792	SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY	GXQ	2013-12-16	View
510(k)	K122647	SYNTHES PATIENT SPECIFIC PLATE	JEY	2013-02-28	View
510(k)	K113567	SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM	JEY	2012-11-19	View
510(k)	K121502	SYNTHES CURVILINEAR DISTRACTION SYSTEM	MQN	2012-08-23	View
510(k)	K121574	SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM	JEY	2012-06-29	View
510(k)	K113251	SYNTHES MATRIXMANDIBLE PERFORMED RECONSTRUCTION PLATES	JEY	2011-12-21	View
510(k)	K111323	SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS	KKY	2011-11-16	View
510(k)	K112689	SYNTHES STERNAL FIXATION SYSTEM	HRS	2011-10-26	View

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