FDA 510(k) Applications Submitted by VILEX, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K102413 |
08/24/2010 |
FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL |
VILEX, INC. |
| K070052 |
01/04/2007 |
MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION |
VILEX, INC. |
| K041287 |
05/13/2004 |
VILEX BONE PLATE SYSTEM |
VILEX, INC. |
| K041289 |
05/13/2004 |
TALUS OF VILEX (TOV) |
VILEX, INC. |
| K052196 |
08/11/2005 |
VILEX X-FIX |
VILEX, INC. |
| K973309 |
09/03/1997 |
VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW |
VILEX, INC. |
| K132820 |
09/09/2013 |
VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES |
VILEX, INC. |
| K023684 |
11/01/2002 |
CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365 |
VILEX, INC. |
| K991151 |
04/06/1999 |
VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW |
VILEX, INC. |
| K991197 |
04/07/1999 |
VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24 |
VILEX, INC. |
| K014154 |
12/18/2001 |
VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00 |
VILEX, INC. |
| K102401 |
08/24/2010 |
HEMI IMPLANT; MINI HEMI IMPLANT |
VILEX, INC. |
| K112837 |
09/28/2011 |
VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE) |
VILEX, INC. |
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