FDA 510(k) Applications Submitted by HENRY QUELLO

FDA 510(k) Number Submission Date Device Name Applicant
K913561 08/09/1991 LUQUE SEGMENTAL SPINAL INSTRUMENTATION ZIMMER, INC.
K860356 01/30/1986 ORTHOBLEND POWERED BONE MILL ZIMMER, INC.
K883665 08/26/1988 COONRAD III TOTAL ELBOW ZIMMER, INC.
K843778 09/25/1984 MAYO ELBOW II ZIMMER, INC.
K925635 11/09/1992 TORUS EXTERNAL FIXATION SYSTEM ZIMMER, INC.


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