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FDA 510(k) Applications Submitted by DENNY STEGER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060680
03/15/2006
ATRILAZE SURGICAL ABLATION SYSTEM
MEDICALCV, INC.
K040744
03/23/2004
ATRILAZE SOFT TISSUE ABLATION SYSTEM
MEDICALCV, INC.
K061489
05/31/2006
ATRILAZE MI SURGICAL ABLATION SYSTEM
MEDICALCV, INC.
K052495
09/12/2005
ATRILAZE MALLEABLE ABLATION PROBE
MEDICALCV, INC.
K033685
11/24/2003
NORTHRUP UNIVERSAL ANNULOPLASTY SYSTEM, MODEL 1000
MEDICALCV, INC.
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