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U&I Corp.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K120419	DYNA LOCKING ANKLE NAIL	HSB	2012-05-21	View
510(k)	K112240	DYNA LOCKING CANNULATED SCREW	HWC	2012-01-04	View
510(k)	K102367	OPTIGEN TOTAL KNEE SYSTEM	JWH	2010-12-08	View
510(k)	K093707	DYNA LOCKING TROCHANTERIC NAIL, MODEL NG0820	HSB	2010-06-23	View
510(k)	K092771	DYNA LOCKING IM NAIL	HSB	2009-12-02	View
510(k)	K091725	PERFIX SPINAL SYSTEM, MODEL SNA4530-9610, SNM4530-9610, SN3020 (TOTAL: 549)	MNH	2009-11-09	View
510(k)	K061002	MAXIMA ANTERIOR CERVICAL PLATE SYSTEM	KWQ	2006-11-15	View
510(k)	K051971	OPTIMA SPINAL SYSTEM	KWQ	2005-08-04	View
510(k)	K042928	MODIFICATION TO GLOBAL SPINAL FIXATION SYSTEM	MNH	2005-02-17	View

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