FDA 510(k) Applications Submitted by LINVATEC CORPORATION D/B/A CONMED LINVATEC

FDA 510(k) Number Submission Date Device Name Applicant
K112965 10/05/2011 NANO SUTURE ANCHOR LINVATEC CORPORATION D/B/A CONMED LINVATEC
K130497 02/26/2013 D4000 DRIVE SYSTEM; D4000A DRIVE SYSTEM WITH IRRIGATION LINVATEC CORPORATION D/B/A CONMED LINVATEC
K131035 04/12/2013 Y-KNOT FLEX ALL-SUTURE ANCHOR, W/ TWO #2 (5 METRIC) HI-FI SUTURES, 1.8MM LINVATEC CORPORATION D/B/A CONMED LINVATEC
K121890 06/28/2012 GENESYS PRESSFT SUTURE ANCHOR LINVATEC CORPORATION D/B/A CONMED LINVATEC


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