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FDA 510(k) Applications Submitted by KRISTYN R 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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