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Vilex, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K112837	VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE)	JDR	2012-10-09	View
510(k)	K102413	FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL	HSB	2011-11-14	View
510(k)	K102401	HEMI IMPLANT; MINI HEMI IMPLANT	KWD	2011-07-20	View
510(k)	K070052	MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION	KWD	2007-03-28	View
510(k)	K052196	VILEX X-FIX	KTT	2005-11-22	View
510(k)	K041287	VILEX BONE PLATE SYSTEM	HWC	2004-08-05	View
510(k)	K041289	TALUS OF VILEX (TOV)	HWC	2004-08-05	View
510(k)	K023684	CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365	KWD	2004-03-01	View
510(k)	K014154	VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00	HWC	2002-03-18	View
510(k)	K991197	VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24	HWC	1999-04-26	View
510(k)	K991151	VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW	HWC	1999-04-26	View
510(k)	K973309	VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW	HWC	1998-01-16	View

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