FDA 510(k) Applications Submitted by KRISTYN R KELLEY

FDA 510(k) Number Submission Date Device Name Applicant
K000348 02/03/2000 COLORADO MICRODISSECTION NEEDLE STRYKER LEIBINGER
K000349 02/03/2000 MOTORIZED MICRO MULTILEAF COLLIMATOR STRYKER LEIBINGER
K991398 04/22/1999 BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KIT STRYKER LEIBINGER
K993990 11/24/1999 LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM STRYKER INSTRUMENTS


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