FDA 510(k) Applications Submitted by ANULEX TECHNOLOGIES, INC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K100572 |
03/01/2010 |
VERSACLOSE, MODEL VC-200-01 |
ANULEX TECHNOLOGIES, INC |
K121354 |
05/04/2012 |
MICRO/MINI N-PK(F) BONE ANCHOR |
ANULEX TECHNOLOGIES, INC |
K121356 |
05/04/2012 |
MICRO/MINI N-PK(H) BONE ANCHOR |
ANULEX TECHNOLOGIES, INC |
K091432 |
05/14/2009 |
XCLOSE TISSUE REPAIR SYSTEM, MODEL XC-200-01 |
ANULEX TECHNOLOGIES, INC |
K111462 |
05/26/2011 |
FIXATE TISSUE BAND |
ANULEX TECHNOLOGIES, INC |
K082729 |
09/18/2008 |
RIMCLOSE BONE ANCHOR |
ANULEX TECHNOLOGIES, INC |
K112849 |
09/29/2011 |
FIXATE TISSUE BAND |
ANULEX TECHNOLOGIES, INC |
K113400 |
11/17/2011 |
FIXATE TISSUE BAND |
ANULEX TECHNOLOGIES, INC |
K113805 |
12/23/2011 |
FIXATE TISSUE BAND |
ANULEX TECHNOLOGIES, INC |
K050969 |
04/18/2005 |
INCLOSE SURGICAL MESH SYSTEM |
ANULEX TECHNOLOGIES, INC |
K061386 |
05/18/2006 |
ANCHOR BAND SUTURING SYSTEM, MODEL SR-AB |
ANULEX TECHNOLOGIES, INC |
K062307 |
08/08/2006 |
XCLOSE TISSUE REPAIR SYSTEM, MODEL SRS |
ANULEX TECHNOLOGIES, INC |
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