FDA 510(k) Applications Submitted by JEFF MILLER

FDA 510(k) Number Submission Date Device Name Applicant
K101126 04/22/2010 PONTIS SUTURES AND SUTURE ANCHORS WITH OPTIONAL CRIMPS CORE ESSENCE ORTHOPAEDICS, INC.
K111716 06/20/2011 KNOTLESS SUTURE FIXATION SYSTEM CORE ESSENCE ORTHOPAEDICS
K011383 05/07/2001 MICRODOSE CATH, MODELS 90121-201, -202, -203 DURECT CORP.
K974848 12/29/1997 MINI-CISER HOUGEN MFG., INC.
K974849 12/29/1997 X-AIR-CISER HOUGEN MFG., INC.


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