FDA 510(k) Applications Submitted by ABRAHAM LAVI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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. |
| K141937 |
07/17/2014 |
TRIDENT FUSION IMPLANT |
VILEX IN TENNESSEE, 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. |
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