FDA 510(k) Applications Submitted by MARTHA MILLER

FDA 510(k) Number Submission Date Device Name Applicant
K963313 08/22/1996 EXACTECH ALL POLY ACETABULAR CUP EXACTECH, INC.
K964262 10/25/1996 EXACTECH TOTAL HIP SYSTME: 22MM FEMORAL HEAD EXACTECH, INC.
K960538 02/07/1996 OPTEON UNIPOLAR EXACTECH, INC.
K960720 02/22/1996 EXACTECH STERILE MODULAR DRILL BIT EXACTECH, INC.
K961304 04/04/1996 AURA HIP SYSTEM CEMENTED FEMORAL STEM/CEMENTED LONG FEMORAL STEM EXACTECH, INC.
K962002 05/22/1996 AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEM EXACTECH, INC.
K954208 09/07/1995 OPTETRAK CONSTRAINED CONDYLAR KNEE FOR CEMENTED USE ONLY EXACTECH, INC.


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