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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