FDA 510(k) Applications Submitted by ABRAHIM LAVI
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
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. |
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