FDA 510(k) Applications Submitted by NANCY HOFT

FDA 510(k) Number Submission Date Device Name Applicant
K140328 02/10/2014 CMC MINI TIGHTROPE ARTHREX, INC.
K071032 04/11/2007 ARTHREX UNIVERS II SHOULDER PROSTHESIS ARTHREX, INC.
K062679 09/08/2006 ARTHREX CORKSCREW FT III SUTURE ANCHOR WITH THREE #2 SUTURES ARTHREX, INC.
K082810 09/24/2008 ARTHREX BIO-COMPOSITE SUTURE ANCHORS: ARTHREX BIO-COMPOSITE PUSHLOCK, BIO-COMPOSITE TAK AND BIO-COMPOSITE CORKSCREW ARTHREX, INC.
K063058 10/05/2006 ARTHREX ANATOEMIC PHALANGEAL PROSTHESIS ARTHREX, INC.
K082999 10/08/2008 ARTHREX MENISCAL DART, ARTHREX MENISCAL DARTSTICK, ARTHREX CHONDRAL DART ARTHREX, INC.
K133275 10/24/2013 MINI TIGHTROPE ARTHREX, INC.


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