FDA 510(k) Applications Submitted by RACHEL KENNEDY

FDA 510(k) Number Submission Date Device Name Applicant
K050506 02/28/2005 PRIMASOLO ONE-PIECE IMPLANTS & HEALING CAPS LIFECORE BIOMEDICAL, INC.
K060530 02/28/2006 SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302. LIFECORE BIOMEDICAL, INC.
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
K051614 06/17/2005 PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICS LIFECORE BIOMEDICAL, 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


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