FDA 510(k) Applications Submitted by KRISTYN WASKI

FDA 510(k) Number Submission Date Device Name Applicant
K970911 03/12/1997 LEE PLATE HOWMEDICA LEIBINGER, INC.
K970912 03/12/1997 LEIBINGER SELF-DRILLING SCREW HOWMEDICA LEIBINGER, INC.
K963502 09/03/1996 CSCO FOREHEAD FIXATION SYSTEM HOWMEDICA CORP.
K964649 11/20/1996 VAZQUEZ DINER INTRAORAL DISTRACTION DEVICE HOWMEDICA LEIBINGER, INC.


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