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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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