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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