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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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